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rs137852737

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852737(C;T)
Make rs137852737(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position16565788
GeneFAM134B
is asnp
is mentioned by
dbSNPrs137852737
ebirs137852737
HLIrs137852737
Exacrs137852737
Varsomers137852737
Maprs137852737
PheGenIrs137852737
hapmaprs137852737
1000 genomesrs137852737
hgdprs137852737
ensemblrs137852737
gopubmedrs137852737
geneviewrs137852737
scholarrs137852737
googlers137852737
pharmgkbrs137852737
gwascentralrs137852737
openSNPrs137852737
23andMers137852737
23andMe allrs137852737
SNP Nexus

SNPshotrs137852737
SNPdbers137852737
MSV3drs137852737
GWAS Ctlgrs137852737
Max Magnitude0
OMIM613114
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852737(T;T)
Alt rs137852737(T;T)
Reference rs137852737(C;C)
Significance Pathogenic
Disease Hereditary sensory and autonomic neuropathy type IIB Hereditary sensory and autonomic neuropathy type IIA
Variation info
Gene FAM134B
CLNDBN Hereditary sensory and autonomic neuropathy type IIB Hereditary sensory and autonomic neuropathy type IIA
Reversed 1
HGVS NC_000005.9:g.16565897G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000358.3, RCV000020420.1,


OMIM201300
Desc
Variant
Relatedalso