Rs119485091

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs119485091(C;C)
Make rs119485091(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position81365005
GeneGAN
is asnp
is mentioned by
dbSNPrs119485091
PheGenIrs119485091
nextbiors119485091
hapmaprs119485091
1000 genomesrs119485091
hgdprs119485091
ensemblrs119485091
gopubmedrs119485091
geneviewrs119485091
scholarrs119485091
googlers119485091
pharmgkbrs119485091
gwascentralrs119485091
openSNPrs119485091
23andMers119485091
23andMe allrs119485091
SNP Nexus

SNPshotrs119485091
SNPdbers119485091
MSV3drs119485091
Max Magnitude0
OMIM605379
Desc
Variant0005
Relatedalso
ClinVar
Risk rs119485091(C;C)
Alt rs119485091(C;C)
Reference rs119485091(T;T)
Significance Pathogenic
Disease Giant axonal neuropathy
Variation info
Gene GAN
CLNDBN Giant axonal neuropathy
Reversed 0
HGVS NC_000016.9:g.81398610T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005337.1,