rs1060499646

Orientation

minus

Stabilized

minus

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

Make rs1060499646(A;G)

Make rs1060499646(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

74792667

Gene

TRPM6

is a	snp
is	mentioned by
dbSNP	rs1060499646
dbSNP (classic)	rs1060499646
ClinGen	rs1060499646
ebi	rs1060499646
HLI	rs1060499646
Exac	rs1060499646
Gnomad	rs1060499646
Varsome	rs1060499646
LitVar	rs1060499646
Map	rs1060499646
PheGenI	rs1060499646
Biobank	rs1060499646
1000 genomes	rs1060499646
hgdp	rs1060499646
ensembl	rs1060499646
geneview	rs1060499646
scholar	rs1060499646
google	rs1060499646
pharmgkb	rs1060499646
gwascentral	rs1060499646
openSNP	rs1060499646
23andMe	rs1060499646
SNPshot	rs1060499646
SNPdbe	rs1060499646
MSV3d	rs1060499646
GWAS Ctlg	rs1060499646

Max Magnitude

0

ClinVar
Risk	rs1060499646(G;G)
Alt	rs1060499646(G;G)
Reference	Rs1060499646(A;A)
Significance	Probable-Pathogenic
Disease	Hypomagnesemia 1
Variation	info
Gene	TRPM6
CLNDBN	Hypomagnesemia 1, intestinal
Reversed	1
HGVS	NC_000009.11:g.77407583T>C
CLNSRC
CLNACC	RCV000463560.1,