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rs207482230

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs207482230(C;T)
Make rs207482230(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position100748182
GeneTFG
is asnp
is mentioned by
dbSNPrs207482230
ebirs207482230
HLIrs207482230
Exacrs207482230
Varsomers207482230
Maprs207482230
PheGenIrs207482230
hapmaprs207482230
1000 genomesrs207482230
hgdprs207482230
ensemblrs207482230
gopubmedrs207482230
geneviewrs207482230
scholarrs207482230
googlers207482230
pharmgkbrs207482230
gwascentralrs207482230
openSNPrs207482230
23andMers207482230
23andMe allrs207482230
SNP Nexus

SNPshotrs207482230
SNPdbers207482230
MSV3drs207482230
GWAS Ctlgrs207482230
Max Magnitude0
ClinVar
Risk rs207482230(T;T)
Alt rs207482230(T;T)
Reference rs207482230(C;C)
Significance Pathogenic
Disease Neuropathy not provided
Variation info
Gene TFG
CLNDBN Neuropathy, hereditary motor and sensory, Okinawa type not provided
Reversed 0
HGVS NC_000003.11:g.100467026C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030736.4, RCV000218755.1,