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rs17076812

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17076812(A;G)
Make rs17076812(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position6421917
GeneMCPH1
is asnp
is mentioned by
dbSNPrs17076812
ebirs17076812
HLIrs17076812
Exacrs17076812
Varsomers17076812
Maprs17076812
PheGenIrs17076812
hapmaprs17076812
1000 genomesrs17076812
hgdprs17076812
ensemblrs17076812
gopubmedrs17076812
geneviewrs17076812
scholarrs17076812
googlers17076812
pharmgkbrs17076812
gwascentralrs17076812
openSNPrs17076812
23andMers17076812
23andMe allrs17076812
SNP Nexus

SNPshotrs17076812
SNPdbers17076812
MSV3drs17076812
GWAS Ctlgrs17076812
GMAF0.1212
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19028548] mentioned as potentially affecting grey matter volume, sample size tiny