rs121907897

Orientation

plus

Stabilized

plus

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

Make rs121907897(G;T)

Make rs121907897(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64599687

Gene

SLC22A12

is a	snp
is	mentioned by
dbSNP	rs121907897
dbSNP (classic)	rs121907897
ClinGen	rs121907897
ebi	rs121907897
HLI	rs121907897
Exac	rs121907897
Gnomad	rs121907897
Varsome	rs121907897
LitVar	rs121907897
Map	rs121907897
PheGenI	rs121907897
Biobank	rs121907897
1000 genomes	rs121907897
hgdp	rs121907897
ensembl	rs121907897
geneview	rs121907897
scholar	rs121907897
google	rs121907897
pharmgkb	rs121907897
gwascentral	rs121907897
openSNP	rs121907897
23andMe	rs121907897
SNPshot	rs121907897
SNPdbe	rs121907897
MSV3d	rs121907897
GWAS Ctlg	rs121907897

Max Magnitude

0

OMIM	607096
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121907897(T;T)
Alt	rs121907897(T;T)
Reference	Rs121907897(G;G)
Significance	Pathogenic
Disease	Familial renal hypouricemia
Variation	info
Gene	SLC22A12
CLNDBN	Familial renal hypouricemia
Reversed	0
HGVS	NC_000011.9:g.64367159G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003694.3,