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rs137852736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs137852736(-;-)
Make rs137852736(-;TC)
ReferenceGRCh38 38.1/141
Chromosome5
Position16616953
GeneFAM134B
is asnp
is mentioned by
dbSNPrs137852736
ebirs137852736
HLIrs137852736
Exacrs137852736
Varsomers137852736
Maprs137852736
PheGenIrs137852736
hapmaprs137852736
1000 genomesrs137852736
hgdprs137852736
ensemblrs137852736
gopubmedrs137852736
geneviewrs137852736
scholarrs137852736
googlers137852736
pharmgkbrs137852736
gwascentralrs137852736
openSNPrs137852736
23andMers137852736
23andMe allrs137852736
SNP Nexus

SNPshotrs137852736
SNPdbers137852736
MSV3drs137852736
GWAS Ctlgrs137852736
Max Magnitude0
ClinVar
Risk rs137852736(;)
Alt rs137852736(;)
Reference rs137852736(TC;TC)
Significance Pathogenic
Disease Hereditary sensory and autonomic neuropathy type IIA
Variation info
Gene FAM134B LOC101929524
CLNDBN Hereditary sensory and autonomic neuropathy type IIA
Reversed 1
HGVS NC_000005.9:g.16617062_16617063delGA
CLNSRC ClinVar GeneReviews
CLNACC RCV000020419.1,


OMIM201300
Desc
Variant
Relatedalso