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rs587777789

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777789(G;T)
Make rs587777789(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position100744917
GeneTFG
is asnp
is mentioned by
dbSNPrs587777789
ebirs587777789
HLIrs587777789
Exacrs587777789
Varsomers587777789
Maprs587777789
PheGenIrs587777789
hapmaprs587777789
1000 genomesrs587777789
hgdprs587777789
ensemblrs587777789
gopubmedrs587777789
geneviewrs587777789
scholarrs587777789
googlers587777789
pharmgkbrs587777789
gwascentralrs587777789
openSNPrs587777789
23andMers587777789
23andMe allrs587777789
SNP Nexus

SNPshotrs587777789
SNPdbers587777789
MSV3drs587777789
GWAS Ctlgrs587777789
Max Magnitude0
ClinVar
Risk rs587777789(T;T)
Alt rs587777789(T;T)
Reference rs587777789(G;G)
Significance Pathogenic
Disease Neuropathy
Variation info
Gene TFG
CLNDBN Neuropathy, hereditary motor and sensory, Okinawa type
Reversed 0
HGVS NC_000003.11:g.100463761G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144505.2,