Have questions? Visit https://www.reddit.com/r/SNPedia

rs869320714

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320714(A;A)
Make rs869320714(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35557404
GeneSLFN14
is asnp
is mentioned by
dbSNPrs869320714
ebirs869320714
HLIrs869320714
Exacrs869320714
Varsomers869320714
Maprs869320714
PheGenIrs869320714
hapmaprs869320714
1000 genomesrs869320714
hgdprs869320714
ensemblrs869320714
gopubmedrs869320714
geneviewrs869320714
scholarrs869320714
googlers869320714
pharmgkbrs869320714
gwascentralrs869320714
openSNPrs869320714
23andMers869320714
23andMe allrs869320714
SNP Nexus

SNPshotrs869320714
SNPdbers869320714
MSV3drs869320714
GWAS Ctlgrs869320714
Max Magnitude0
ClinVar
Risk rs869320714(A;A)
Alt rs869320714(A;A)
Reference rs869320714(T;T)
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.33884423A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000210921.1,