rs376324882

Orientation

plus

Stabilized

plus

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

Make rs376324882(A;A)

Make rs376324882(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

40410756

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs376324882
dbSNP (classic)	rs376324882
ClinGen	rs376324882
ebi	rs376324882
HLI	rs376324882
Exac	rs376324882
Gnomad	rs376324882
Varsome	rs376324882
LitVar	rs376324882
Map	rs376324882
PheGenI	rs376324882
Biobank	rs376324882
1000 genomes	rs376324882
hgdp	rs376324882
ensembl	rs376324882
geneview	rs376324882
scholar	rs376324882
google	rs376324882
pharmgkb	rs376324882
gwascentral	rs376324882
openSNP	rs376324882
23andMe	rs376324882
SNPshot	rs376324882
SNPdbe	rs376324882
MSV3d	rs376324882
GWAS Ctlg	rs376324882

Max Magnitude

0

ClinVar
Risk	rs376324882(A;A) rs376324882(T;T)
Alt	rs376324882(A;A) rs376324882(T;T)
Reference	Rs376324882(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40702955C>T
CLNSRC
CLNACC	RCV000185983.1,