rs786205530

Orientation

plus

Stabilized

plus

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

Make rs786205530(C;T)

Make rs786205530(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

96761733

Gene

CNNM4

is a	snp
is	mentioned by
dbSNP	rs786205530
dbSNP (classic)	rs786205530
ClinGen	rs786205530
ebi	rs786205530
HLI	rs786205530
Exac	rs786205530
Gnomad	rs786205530
Varsome	rs786205530
LitVar	rs786205530
Map	rs786205530
PheGenI	rs786205530
Biobank	rs786205530
1000 genomes	rs786205530
hgdp	rs786205530
ensembl	rs786205530
geneview	rs786205530
scholar	rs786205530
google	rs786205530
pharmgkb	rs786205530
gwascentral	rs786205530
openSNP	rs786205530
23andMe	rs786205530
SNPshot	rs786205530
SNPdbe	rs786205530
MSV3d	rs786205530
GWAS Ctlg	rs786205530

Max Magnitude

0

ClinVar
Risk	rs786205530(T;T)
Alt	rs786205530(T;T)
Reference	Rs786205530(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CNNM4
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.97427470C>T
CLNSRC
CLNACC	RCV000171299.1,