SNP Report
Basic Info
Name |
rs7164335
dbSNP
Ensembl
|
Location |
Chr15:68715032(Fwd) |
Variant Alleles |
A/G |
Ancestral Allele |
G |
Functional Annotation |
intron_variant.
|
Consequence to Transcript |
intron_variant(ENST00000423218; ENST00000315757) |
No. of Studies |
1 (significant: 0; non-significant: 0; trend: 1) |
Source |
Literature-origin
|
SNP related studies (count: 1)
SNP related genes (count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.
Literature-origin SNPs (count: 0)
LD-proxies (count: 11)
rs_ID |
Functional Annotation |
r2[population] |
rs8036876
|
intron_variant |
0.955[CEU]; 0.913[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs8036698
|
intron_variant |
0.953[CEU]; 1.0[CHB]; 0.951[JPT]
|
rs4777051
|
intron_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs6494744
|
intron_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs11635776
|
intron_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs7165305
|
intron_variant |
1.0[CEU]; 0.955[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs8036939
|
intron_variant |
0.955[CEU]; 0.913[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs7165618
|
intron_variant |
1.0[CEU]; 0.954[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs7164172
|
intron_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs8038368
|
intron_variant |
0.955[CEU]; 0.913[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs11072021
|
intron_variant |
1.0[YRI]
|