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rs879255268

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255268(A;A)
Make rs879255268(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position37403347
GeneSRC
is asnp
is mentioned by
dbSNPrs879255268
ebirs879255268
HLIrs879255268
Exacrs879255268
Varsomers879255268
Maprs879255268
PheGenIrs879255268
hapmaprs879255268
1000 genomesrs879255268
hgdprs879255268
ensemblrs879255268
gopubmedrs879255268
geneviewrs879255268
scholarrs879255268
googlers879255268
pharmgkbrs879255268
gwascentralrs879255268
openSNPrs879255268
23andMers879255268
23andMe allrs879255268
SNP Nexus

SNPshotrs879255268
SNPdbers879255268
MSV3drs879255268
GWAS Ctlgrs879255268
Max Magnitude0
ClinVar
Risk rs879255268(A;A)
Alt rs879255268(A;A)
Reference rs879255268(G;G)
Significance Pathogenic
Disease Thrombocytopenia 6
Variation info
Gene SRC
CLNDBN Thrombocytopenia 6
Reversed 0
HGVS NC_000020.10:g.36031750G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000211002.1,