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

rs119477056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119477056(C;T)
Make rs119477056(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position111585362
GeneCD96
is asnp
is mentioned by
dbSNPrs119477056
ebirs119477056
HLIrs119477056
Exacrs119477056
Varsomers119477056
Maprs119477056
PheGenIrs119477056
hapmaprs119477056
1000 genomesrs119477056
hgdprs119477056
ensemblrs119477056
gopubmedrs119477056
geneviewrs119477056
scholarrs119477056
googlers119477056
pharmgkbrs119477056
gwascentralrs119477056
openSNPrs119477056
23andMers119477056
23andMe allrs119477056
SNP Nexus

SNPshotrs119477056
SNPdbers119477056
MSV3drs119477056
GWAS Ctlgrs119477056
Max Magnitude0
OMIM606037
Desc
Variant0002
Relatedalso
ClinVar
Risk rs119477056(A,T;A,T)
Alt rs119477056(A,T;A,T)
Reference rs119477056(C;C)
Significance Pathogenic
Disease C syndrome
Variation info
Gene CD96
CLNDBN C syndrome
Reversed 0
HGVS NC_000003.11:g.111304209C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004903.2,