rs757261752

Orientation

plus

Stabilized

plus

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

Make rs757261752(A;C)

Make rs757261752(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

40405828

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs757261752
dbSNP (classic)	rs757261752
ClinGen	rs757261752
ebi	rs757261752
HLI	rs757261752
Exac	rs757261752
Gnomad	rs757261752
Varsome	rs757261752
LitVar	rs757261752
Map	rs757261752
PheGenI	rs757261752
Biobank	rs757261752
1000 genomes	rs757261752
hgdp	rs757261752
ensembl	rs757261752
geneview	rs757261752
scholar	rs757261752
google	rs757261752
pharmgkb	rs757261752
gwascentral	rs757261752
openSNP	rs757261752
23andMe	rs757261752
SNPshot	rs757261752
SNPdbe	rs757261752
MSV3d	rs757261752
GWAS Ctlg	rs757261752

Max Magnitude

0

ClinVar
Risk	rs757261752(C;C) rs757261752(T;T)
Alt	rs757261752(C;C) rs757261752(T;T)
Reference	Rs757261752(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40698029A>C
CLNSRC
CLNACC	RCV000413818.1,