rs121912623

Orientation

minus

Stabilized

minus

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

Make rs121912623(C;T)

Make rs121912623(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

74812322

Gene

TRPM6

is a	snp
is	mentioned by
dbSNP	rs121912623
dbSNP (classic)	rs121912623
ClinGen	rs121912623
ebi	rs121912623
HLI	rs121912623
Exac	rs121912623
Gnomad	rs121912623
Varsome	rs121912623
LitVar	rs121912623
Map	rs121912623
PheGenI	rs121912623
Biobank	rs121912623
1000 genomes	rs121912623
hgdp	rs121912623
ensembl	rs121912623
geneview	rs121912623
scholar	rs121912623
google	rs121912623
pharmgkb	rs121912623
gwascentral	rs121912623
openSNP	rs121912623
23andMe	rs121912623
SNPshot	rs121912623
SNPdbe	rs121912623
MSV3d	rs121912623
GWAS Ctlg	rs121912623

Max Magnitude

0

OMIM	607009
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121912623(T;T)
Alt	rs121912623(T;T)
Reference	Rs121912623(C;C)
Significance	Pathogenic
Disease	Hypomagnesemia 1
Variation	info
Gene	TRPM6
CLNDBN	Hypomagnesemia 1, intestinal
Reversed	1
HGVS	NC_000009.11:g.77427238G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003764.4,