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rs796065025

From SNPedia

Orientationminus
Make rs796065025(-;-)
Make rs796065025(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position75843204
GeneUNC13D
is asnp
is mentioned by
dbSNPrs796065025
ebirs796065025
HLIrs796065025
Exacrs796065025
Varsomers796065025
Maprs796065025
PheGenIrs796065025
hapmaprs796065025
1000 genomesrs796065025
hgdprs796065025
ensemblrs796065025
gopubmedrs796065025
geneviewrs796065025
scholarrs796065025
googlers796065025
pharmgkbrs796065025
gwascentralrs796065025
openSNPrs796065025
23andMers796065025
23andMe allrs796065025
SNP Nexus

SNPshotrs796065025
SNPdbers796065025
MSV3drs796065025
GWAS Ctlgrs796065025
Max Magnitude
ClinVar
Risk rs796065025(;)
Alt rs796065025(;)
Reference rs796065025(C;C)
Significance Pathogenic
Disease Hemophagocytic lymphohistiocytosis
Variation info
Gene UNC13D
CLNDBN Hemophagocytic lymphohistiocytosis, familial, 3
Reversed 1
HGVS NC_000017.10:g.73839285delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000002074.3,