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rs7077164

From SNPedia

Orientationplus
Stabilizedplus
Make rs7077164(C;C)
Make rs7077164(C;T)
Make rs7077164(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position69823442
GeneCOL13A1, LOC105378347
is asnp
is mentioned by
dbSNPrs7077164
dbSNP (classic)rs7077164
ClinGenrs7077164
ebirs7077164
HLIrs7077164
Exacrs7077164
Gnomadrs7077164
Varsomers7077164
LitVarrs7077164
Maprs7077164
PheGenIrs7077164
Biobankrs7077164
1000 genomesrs7077164
hgdprs7077164
ensemblrs7077164
geneviewrs7077164
scholarrs7077164
googlers7077164
pharmgkbrs7077164
gwascentralrs7077164
openSNPrs7077164
23andMers7077164
SNPshotrs7077164
SNPdbers7077164
MSV3drs7077164
GWAS Ctlgrs7077164
GMAF0.3926
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20708005OA-icon.png]
Trait
Title Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
Risk Allele A
P-val 0.000007
Odds Ratio 0.67 [NR] unit increase