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

rs201908137

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201908137(A;A)
Make rs201908137(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position75840506
GeneUNC13D
is asnp
is mentioned by
dbSNPrs201908137
ebirs201908137
HLIrs201908137
Exacrs201908137
Varsomers201908137
Maprs201908137
PheGenIrs201908137
hapmaprs201908137
1000 genomesrs201908137
hgdprs201908137
ensemblrs201908137
gopubmedrs201908137
geneviewrs201908137
scholarrs201908137
googlers201908137
pharmgkbrs201908137
gwascentralrs201908137
openSNPrs201908137
23andMers201908137
23andMe allrs201908137
SNP Nexus

SNPshotrs201908137
SNPdbers201908137
MSV3drs201908137
GWAS Ctlgrs201908137
Max Magnitude0
ClinVar
Risk rs201908137(A;A)
Alt rs201908137(A;A)
Reference rs201908137(C;C)
Significance Pathogenic
Disease Hemophagocytic lymphohistiocytosis
Variation info
Gene UNC13D
CLNDBN Hemophagocytic lymphohistiocytosis, familial, 3
Reversed 0
HGVS NC_000017.10:g.73836587C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002078.3,