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rs1060505056

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs1060505056(-;-)
Make rs1060505056(-;AT)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position39138665
GeneFYB
is asnp
is mentioned by
dbSNPrs1060505056
dbSNP (old)rs1060505056
ClinGenrs1060505056
ebirs1060505056
HLIrs1060505056
Exacrs1060505056
Gnomadrs1060505056
Varsomers1060505056
Maprs1060505056
PheGenIrs1060505056
Biobankrs1060505056
1000 genomesrs1060505056
hgdprs1060505056
ensemblrs1060505056
gopubmedrs1060505056
geneviewrs1060505056
scholarrs1060505056
googlers1060505056
pharmgkbrs1060505056
gwascentralrs1060505056
openSNPrs1060505056
23andMers1060505056
23andMe allrs1060505056
SNPshotrs1060505056
SNPdbers1060505056
MSV3drs1060505056
GWAS Ctlgrs1060505056
Max Magnitude0
ClinVar
Risk rs1060505056(-;-)
Alt rs1060505056(-;-)
Reference Rs1060505056(AT;AT)
Significance Pathogenic
Disease Thrombocytopenia 3
Variation info
Gene FYB
CLNDBN Thrombocytopenia 3
Reversed 1
HGVS NC_000005.9:g.39138767_39138768delAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000477971.1,