rs150855952

Orientation

plus

Stabilized

plus

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

Make rs150855952(A;A)

Make rs150855952(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

40418234

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs150855952
dbSNP (classic)	rs150855952
ClinGen	rs150855952
ebi	rs150855952
HLI	rs150855952
Exac	rs150855952
Gnomad	rs150855952
Varsome	rs150855952
LitVar	rs150855952
Map	rs150855952
PheGenI	rs150855952
Biobank	rs150855952
1000 genomes	rs150855952
hgdp	rs150855952
ensembl	rs150855952
geneview	rs150855952
scholar	rs150855952
google	rs150855952
pharmgkb	rs150855952
gwascentral	rs150855952
openSNP	rs150855952
23andMe	rs150855952
SNPshot	rs150855952
SNPdbe	rs150855952
MSV3d	rs150855952
GWAS Ctlg	rs150855952

Max Magnitude

0

ClinVar
Risk	rs150855952(A;A)
Alt	rs150855952(A;A)
Reference	Rs150855952(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	IVD
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.40710433G>A
CLNSRC
CLNACC	RCV000185978.1,