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rs77542162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common genotype
Make rs77542162(A;G)
Make rs77542162(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position69085137
GeneABCA6
is asnp
is mentioned by
dbSNPrs77542162
dbSNP (classic)rs77542162
ClinGenrs77542162
ebirs77542162
HLIrs77542162
Exacrs77542162
Gnomadrs77542162
Varsomers77542162
LitVarrs77542162
Maprs77542162
PheGenIrs77542162
Biobankrs77542162
1000 genomesrs77542162
hgdprs77542162
ensemblrs77542162
geneviewrs77542162
scholarrs77542162
googlers77542162
pharmgkbrs77542162
gwascentralrs77542162
openSNPrs77542162
23andMers77542162
23andMe allrs77542162
SNPshotrs77542162
SNPdbers77542162
MSV3drs77542162
GWAS Ctlgrs77542162
Max Magnitude0

[PMID 28146470OA-icon.png] Rare and low-frequency coding variants alter human adult height.