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rs193302875

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193302875(G;T)
Make rs193302875(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position70598558
GenePRF1
is asnp
is mentioned by
dbSNPrs193302875
ebirs193302875
HLIrs193302875
Exacrs193302875
Varsomers193302875
Maprs193302875
PheGenIrs193302875
hapmaprs193302875
1000 genomesrs193302875
hgdprs193302875
ensemblrs193302875
gopubmedrs193302875
geneviewrs193302875
scholarrs193302875
googlers193302875
pharmgkbrs193302875
gwascentralrs193302875
openSNPrs193302875
23andMers193302875
23andMe allrs193302875
SNP Nexus

SNPshotrs193302875
SNPdbers193302875
MSV3drs193302875
GWAS Ctlgrs193302875
Max Magnitude0
ClinVar
Risk rs193302875(T;T)
Alt rs193302875(T;T)
Reference rs193302875(G;G)
Significance Pathogenic
Disease Aplastic anemia
Variation info
Gene PRF1
CLNDBN Aplastic anemia
Reversed 1
HGVS NC_000010.10:g.72358314C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014722.22,