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

rs119485094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119485094(C;T)
Make rs119485094(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position81365405
GeneGAN
is asnp
is mentioned by
dbSNPrs119485094
ebirs119485094
HLIrs119485094
Exacrs119485094
Varsomers119485094
Maprs119485094
PheGenIrs119485094
hapmaprs119485094
1000 genomesrs119485094
hgdprs119485094
ensemblrs119485094
gopubmedrs119485094
geneviewrs119485094
scholarrs119485094
googlers119485094
pharmgkbrs119485094
gwascentralrs119485094
openSNPrs119485094
23andMers119485094
23andMe allrs119485094
SNP Nexus

SNPshotrs119485094
SNPdbers119485094
MSV3drs119485094
GWAS Ctlgrs119485094
Max Magnitude0
OMIM605379
Desc
Variant0008
Relatedalso
ClinVar
Risk rs119485094(T;T)
Alt rs119485094(T;T)
Reference rs119485094(C;C)
Significance Pathogenic
Disease Giant axonal neuropathy
Variation info
Gene GAN
CLNDBN Giant axonal neuropathy
Reversed 0
HGVS NC_000016.9:g.81399010C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005340.3,