Rs119485090

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119485090(C;T)
Make rs119485090(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position81354723
GeneGAN
is asnp
is mentioned by
dbSNPrs119485090
Exacrs119485090
PheGenIrs119485090
nextbiors119485090
hapmaprs119485090
1000 genomesrs119485090
hgdprs119485090
ensemblrs119485090
gopubmedrs119485090
geneviewrs119485090
scholarrs119485090
googlers119485090
pharmgkbrs119485090
gwascentralrs119485090
openSNPrs119485090
23andMers119485090
23andMe allrs119485090
SNP Nexus

SNPshotrs119485090
SNPdbers119485090
MSV3drs119485090
OMIM605379
Desc
Variant0004
Relatedalso
ClinVar
Risk rs119485090(T;T)
Alt rs119485090(T;T)
Reference rs119485090(C;C)
Significance Pathogenic
Disease Giant axonal neuropathy
Variation info
Gene GAN
CLNDBN Giant axonal neuropathy
Reversed 0
HGVS NC_000016.9:g.81388328C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005336.1,