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rs121908936

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 5 Congenital lactase deficiency
(A;T) 2.5 Carrier of a congenital lactase deficiency allele
(T;T) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome2
Position135807131
GeneLCT
is asnp
is mentioned by
dbSNPrs121908936
ebirs121908936
HLIrs121908936
Exacrs121908936
Varsomers121908936
Maprs121908936
PheGenIrs121908936
hapmaprs121908936
1000 genomesrs121908936
hgdprs121908936
ensemblrs121908936
gopubmedrs121908936
geneviewrs121908936
scholarrs121908936
googlers121908936
pharmgkbrs121908936
gwascentralrs121908936
openSNPrs121908936
23andMers121908936
23andMe allrs121908936
SNP Nexus

SNPshotrs121908936
SNPdbers121908936
MSV3drs121908936
GWAS Ctlgrs121908936
Max Magnitude5
OMIM603202
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908936(A;A)
Alt rs121908936(A;A)
Reference rs121908936(T;T)
Significance Pathogenic
Disease Congenital lactase deficiency
Variation info
Gene LCT
CLNDBN Congenital lactase deficiency
Reversed 1
HGVS NC_000002.11:g.136564701A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006964.2,