rs398123679

Orientation

plus

Stabilized

plus

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

Make rs398123679(A;A)

Make rs398123679(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

40416290

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs398123679
dbSNP (classic)	rs398123679
ClinGen	rs398123679
ebi	rs398123679
HLI	rs398123679
Exac	rs398123679
Gnomad	rs398123679
Varsome	rs398123679
LitVar	rs398123679
Map	rs398123679
PheGenI	rs398123679
Biobank	rs398123679
1000 genomes	rs398123679
hgdp	rs398123679
ensembl	rs398123679
geneview	rs398123679
scholar	rs398123679
google	rs398123679
pharmgkb	rs398123679
gwascentral	rs398123679
openSNP	rs398123679
23andMe	rs398123679
SNPshot	rs398123679
SNPdbe	rs398123679
MSV3d	rs398123679
GWAS Ctlg	rs398123679

Max Magnitude

0

ClinVar
Risk	rs398123679(A;A)
Alt	rs398123679(A;A)
Reference	Rs398123679(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	IVD
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000015.9:g.40708489G>A
CLNSRC
CLNACC	RCV000185976.3, RCV000417380.1,