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rs869320715

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869320715(A;T)
Make rs869320715(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35557406
GeneSLFN14
is asnp
is mentioned by
dbSNPrs869320715
ebirs869320715
HLIrs869320715
Exacrs869320715
Varsomers869320715
Maprs869320715
PheGenIrs869320715
hapmaprs869320715
1000 genomesrs869320715
hgdprs869320715
ensemblrs869320715
gopubmedrs869320715
geneviewrs869320715
scholarrs869320715
googlers869320715
pharmgkbrs869320715
gwascentralrs869320715
openSNPrs869320715
23andMers869320715
23andMe allrs869320715
SNP Nexus

SNPshotrs869320715
SNPdbers869320715
MSV3drs869320715
GWAS Ctlgrs869320715
Max Magnitude0
ClinVar
Risk rs869320715(T;T)
Alt rs869320715(T;T)
Reference rs869320715(A;A)
Significance Pathogenic
Disease Platelet-type bleeding disorder 20
Variation info
Gene SLFN14
CLNDBN Platelet-type bleeding disorder 20
Reversed 1
HGVS NC_000017.10:g.33884425T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210923.1,