rs121912622

Orientation

minus

Stabilized

minus

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

Make rs121912622(C;G)

Make rs121912622(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

74802138

Gene

TRPM6

is a	snp
is	mentioned by
dbSNP	rs121912622
dbSNP (classic)	rs121912622
ClinGen	rs121912622
ebi	rs121912622
HLI	rs121912622
Exac	rs121912622
Gnomad	rs121912622
Varsome	rs121912622
LitVar	rs121912622
Map	rs121912622
PheGenI	rs121912622
Biobank	rs121912622
1000 genomes	rs121912622
hgdp	rs121912622
ensembl	rs121912622
geneview	rs121912622
scholar	rs121912622
google	rs121912622
pharmgkb	rs121912622
gwascentral	rs121912622
openSNP	rs121912622
23andMe	rs121912622
SNPshot	rs121912622
SNPdbe	rs121912622
MSV3d	rs121912622
GWAS Ctlg	rs121912622

Max Magnitude

0

OMIM	607009
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121912622(G;G)
Alt	rs121912622(G;G)
Reference	Rs121912622(C;C)
Significance	Pathogenic
Disease	Hypomagnesemia 1
Variation	info
Gene	TRPM6
CLNDBN	Hypomagnesemia 1, intestinal
Reversed	1
HGVS	NC_000009.11:g.77417054G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003758.3,