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rs374239531

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374239531(C;G)
Make rs374239531(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150133957
GenePDGFRB
is asnp
is mentioned by
dbSNPrs374239531
ebirs374239531
HLIrs374239531
Exacrs374239531
Varsomers374239531
Maprs374239531
PheGenIrs374239531
hapmaprs374239531
1000 genomesrs374239531
hgdprs374239531
ensemblrs374239531
gopubmedrs374239531
geneviewrs374239531
scholarrs374239531
googlers374239531
pharmgkbrs374239531
gwascentralrs374239531
openSNPrs374239531
23andMers374239531
23andMe allrs374239531
SNP Nexus

SNPshotrs374239531
SNPdbers374239531
MSV3drs374239531
GWAS Ctlgrs374239531
Max Magnitude0
ClinVar
Risk rs374239531(G;G)
Alt rs374239531(G;G)
Reference rs374239531(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDGFRB
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.149513520C>T
CLNSRC
CLNACC RCV000171387.1,