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rs199714731

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199714731(A;A)
Make rs199714731(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position28552493
GeneUNC119
is asnp
is mentioned by
dbSNPrs199714731
ebirs199714731
HLIrs199714731
Exacrs199714731
Varsomers199714731
Maprs199714731
PheGenIrs199714731
hapmaprs199714731
1000 genomesrs199714731
hgdprs199714731
ensemblrs199714731
gopubmedrs199714731
geneviewrs199714731
scholarrs199714731
googlers199714731
pharmgkbrs199714731
gwascentralrs199714731
openSNPrs199714731
23andMers199714731
23andMe allrs199714731
SNP Nexus

SNPshotrs199714731
SNPdbers199714731
MSV3drs199714731
GWAS Ctlgrs199714731
Max Magnitude0
ClinVar
Risk rs199714731(A;A)
Alt rs199714731(A;A)
Reference rs199714731(C;C)
Significance Pathogenic
Disease Immunodeficiency 13
Variation info
Gene UNC119
CLNDBN Immunodeficiency 13
Reversed 0
HGVS NC_000017.10:g.26879511C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074396.4,