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rs137852738

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852738(C;C)
Make rs137852738(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position16478032
GeneFAM134B
is asnp
is mentioned by
dbSNPrs137852738
ebirs137852738
HLIrs137852738
Exacrs137852738
Varsomers137852738
Maprs137852738
PheGenIrs137852738
hapmaprs137852738
1000 genomesrs137852738
hgdprs137852738
ensemblrs137852738
gopubmedrs137852738
geneviewrs137852738
scholarrs137852738
googlers137852738
pharmgkbrs137852738
gwascentralrs137852738
openSNPrs137852738
23andMers137852738
23andMe allrs137852738
SNP Nexus

SNPshotrs137852738
SNPdbers137852738
MSV3drs137852738
GWAS Ctlgrs137852738
Max Magnitude0
ClinVar
Risk rs137852738(C;C)
Alt rs137852738(C;C)
Reference rs137852738(T;T)
Significance Pathogenic
Disease Hereditary sensory and autonomic neuropathy type IIA
Variation info
Gene FAM134B
CLNDBN Hereditary sensory and autonomic neuropathy type IIA
Reversed 1
HGVS NC_000005.9:g.16478141A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020421.1,


OMIM201300
Desc
Variant
Relatedalso