rs374239531

Orientation

plus

Stabilized

plus

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

Make rs374239531(C;G)

Make rs374239531(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

150133957

Gene

PDGFRB

is a	snp
is	mentioned by
dbSNP	rs374239531
dbSNP (classic)	rs374239531
ClinGen	rs374239531
ebi	rs374239531
HLI	rs374239531
Exac	rs374239531
Gnomad	rs374239531
Varsome	rs374239531
LitVar	rs374239531
Map	rs374239531
PheGenI	rs374239531
Biobank	rs374239531
1000 genomes	rs374239531
hgdp	rs374239531
ensembl	rs374239531
geneview	rs374239531
scholar	rs374239531
google	rs374239531
pharmgkb	rs374239531
gwascentral	rs374239531
openSNP	rs374239531
23andMe	rs374239531
SNPshot	rs374239531
SNPdbe	rs374239531
MSV3d	rs374239531
GWAS Ctlg	rs374239531

Max Magnitude

0

ClinVar
Risk	rs374239531(G;G) rs374239531(T;T)
Alt	rs374239531(G;G) rs374239531(T;T)
Reference	Rs374239531(C;C)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	PDGFRB
CLNDBN	not specified
Reversed	0
HGVS	NC_000005.9:g.149513520C>T
CLNSRC
CLNACC	RCV000171387.2,