rs121908937

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	5	Congenital lactase deficiency
(C;G)	2.5	Carrier of a congenital lactase deficiency allele
(G;G)	0	common in clinvar

Reference

GRCh38 38.1/141

Chromosome

2

Position

135829593

Gene

LCT

is a	snp
is	mentioned by
dbSNP	rs121908937
dbSNP (classic)	rs121908937
ClinGen	rs121908937
ebi	rs121908937
HLI	rs121908937
Exac	rs121908937
Gnomad	rs121908937
Varsome	rs121908937
LitVar	rs121908937
Map	rs121908937
PheGenI	rs121908937
Biobank	rs121908937
1000 genomes	rs121908937
hgdp	rs121908937
ensembl	rs121908937
geneview	rs121908937
scholar	rs121908937
google	rs121908937
pharmgkb	rs121908937
gwascentral	rs121908937
openSNP	rs121908937
23andMe	rs121908937
SNPshot	rs121908937
SNPdbe	rs121908937
MSV3d	rs121908937
GWAS Ctlg	rs121908937

Max Magnitude

5

OMIM	603202
Desc
Variant	0003
Related	also

ClinVar
Risk	Rs121908937(C;C)
Alt	Rs121908937(C;C)
Reference	Rs121908937(G;G)
Significance	Pathogenic
Disease	Congenital lactase deficiency
Variation	info
Gene	LCT
CLNDBN	Congenital lactase deficiency
Reversed	1
HGVS	NC_000002.11:g.136587163C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006966.2,