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rs1163623

From SNPedia

Orientationplus
Stabilizedplus
Make rs1163623(C;C)
Make rs1163623(C;T)
Make rs1163623(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position111569284
is asnp
is mentioned by
dbSNPrs1163623
dbSNP (classic)rs1163623
ClinGenrs1163623
ebirs1163623
HLIrs1163623
Exacrs1163623
Gnomadrs1163623
Varsomers1163623
LitVarrs1163623
Maprs1163623
PheGenIrs1163623
Biobankrs1163623
1000 genomesrs1163623
hgdprs1163623
ensemblrs1163623
geneviewrs1163623
scholarrs1163623
googlers1163623
pharmgkbrs1163623
gwascentralrs1163623
openSNPrs1163623
23andMers1163623
SNPshotrs1163623
SNPdbers1163623
MSV3drs1163623
GWAS Ctlgrs1163623
GMAF0.1327
Max Magnitude0
? (C;C) (C;T) (T;T) 28


OMIM300488
DescMENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 1; MENOQ1
Variant
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