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rs757188030

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757188030(A;A)
Make rs757188030(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position35557396
GeneSLFN14
is asnp
is mentioned by
dbSNPrs757188030
ebirs757188030
HLIrs757188030
Exacrs757188030
Varsomers757188030
Maprs757188030
PheGenIrs757188030
hapmaprs757188030
1000 genomesrs757188030
hgdprs757188030
ensemblrs757188030
gopubmedrs757188030
geneviewrs757188030
scholarrs757188030
googlers757188030
pharmgkbrs757188030
gwascentralrs757188030
openSNPrs757188030
23andMers757188030
23andMe allrs757188030
SNP Nexus

SNPshotrs757188030
SNPdbers757188030
MSV3drs757188030
GWAS Ctlgrs757188030
Max Magnitude0
ClinVar
Risk rs757188030(A;A)
Alt rs757188030(A;A)
Reference rs757188030(G;G)
Significance Pathogenic
Disease Platelet-type bleeding disorder 20
Variation info
Gene SLFN14
CLNDBN Platelet-type bleeding disorder 20
Reversed 0
HGVS NC_000017.10:g.33884415G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210922.1,