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rs869320716

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869320716(A;G)
Make rs869320716(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35557411
GeneSLFN14
is asnp
is mentioned by
dbSNPrs869320716
ebirs869320716
HLIrs869320716
Exacrs869320716
Varsomers869320716
Maprs869320716
PheGenIrs869320716
hapmaprs869320716
1000 genomesrs869320716
hgdprs869320716
ensemblrs869320716
gopubmedrs869320716
geneviewrs869320716
scholarrs869320716
googlers869320716
pharmgkbrs869320716
gwascentralrs869320716
openSNPrs869320716
23andMers869320716
23andMe allrs869320716
SNP Nexus

SNPshotrs869320716
SNPdbers869320716
MSV3drs869320716
GWAS Ctlgrs869320716
Max Magnitude0
ClinVar
Risk rs869320716(G;G)
Alt rs869320716(G;G)
Reference rs869320716(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.33884430T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210920.1,