rs121909386

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121909386(C;T)

Make rs121909386(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

89438899

Gene

SLC16A12

is a	snp
is	mentioned by
dbSNP	rs121909386
dbSNP (classic)	rs121909386
ClinGen	rs121909386
ebi	rs121909386
HLI	rs121909386
Exac	rs121909386
Gnomad	rs121909386
Varsome	rs121909386
LitVar	rs121909386
Map	rs121909386
PheGenI	rs121909386
Biobank	rs121909386
1000 genomes	rs121909386
hgdp	rs121909386
ensembl	rs121909386
geneview	rs121909386
scholar	rs121909386
google	rs121909386
pharmgkb	rs121909386
gwascentral	rs121909386
openSNP	rs121909386
23andMe	rs121909386
SNPshot	rs121909386
SNPdbe	rs121909386
MSV3d	rs121909386
GWAS Ctlg	rs121909386

Max Magnitude

0

OMIM	611910
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909386(T;T)
Alt	rs121909386(T;T)
Reference	Rs121909386(C;C)
Significance	Pathogenic
Disease	Cataract
Variation	info
Gene	SLC16A12
CLNDBN	Cataract, juvenile, with microcornea and glucosuria
Reversed	1
HGVS	NC_000010.10:g.91198656G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000820.5,