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rs797044887

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044887(A;C)
Make rs797044887(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position150124277
GenePDGFRB
is asnp
is mentioned by
dbSNPrs797044887
ebirs797044887
HLIrs797044887
Exacrs797044887
Varsomers797044887
Maprs797044887
PheGenIrs797044887
hapmaprs797044887
1000 genomesrs797044887
hgdprs797044887
ensemblrs797044887
gopubmedrs797044887
geneviewrs797044887
scholarrs797044887
googlers797044887
pharmgkbrs797044887
gwascentralrs797044887
openSNPrs797044887
23andMers797044887
23andMe allrs797044887
SNP Nexus

SNPshotrs797044887
SNPdbers797044887
MSV3drs797044887
GWAS Ctlgrs797044887
Max Magnitude0
ClinVar
Risk rs797044887(C;C)
Alt rs797044887(C;C)
Reference rs797044887(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PDGFRB
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000005.9:g.149503840T>G
CLNSRC
CLNACC RCV000190709.1,