rs387906975

Orientation

plus

Stabilized

plus

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

Make rs387906975(C;T)

Make rs387906975(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

103049788

Gene

CNNM2

is a	snp
is	mentioned by
dbSNP	rs387906975
dbSNP (classic)	rs387906975
ClinGen	rs387906975
ebi	rs387906975
HLI	rs387906975
Exac	rs387906975
Gnomad	rs387906975
Varsome	rs387906975
LitVar	rs387906975
Map	rs387906975
PheGenI	rs387906975
Biobank	rs387906975
1000 genomes	rs387906975
hgdp	rs387906975
ensembl	rs387906975
geneview	rs387906975
scholar	rs387906975
google	rs387906975
pharmgkb	rs387906975
gwascentral	rs387906975
openSNP	rs387906975
23andMe	rs387906975
SNPshot	rs387906975
SNPdbe	rs387906975
MSV3d	rs387906975
GWAS Ctlg	rs387906975

Max Magnitude

0

ClinVar
Risk	rs387906975(T;T)
Alt	rs387906975(T;T)
Reference	Rs387906975(C;C)
Significance	Pathogenic
Disease	Hypomagnesemia 6
Variation	info
Gene	CNNM2
CLNDBN	Hypomagnesemia 6, renal
Reversed	0
HGVS	NC_000010.10:g.104809545C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023661.2,