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rs1085307142

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome3
Position38909109
GeneSCN11A
is asnp
is mentioned by
dbSNPrs1085307142
dbSNP (old)rs1085307142
ClinGenrs1085307142
ebirs1085307142
HLIrs1085307142
Exacrs1085307142
Gnomadrs1085307142
Varsomers1085307142
Maprs1085307142
PheGenIrs1085307142
Biobankrs1085307142
1000 genomesrs1085307142
hgdprs1085307142
ensemblrs1085307142
gopubmedrs1085307142
geneviewrs1085307142
scholarrs1085307142
googlers1085307142
pharmgkbrs1085307142
gwascentralrs1085307142
openSNPrs1085307142
23andMers1085307142
23andMe allrs1085307142
SNPshotrs1085307142
SNPdbers1085307142
MSV3drs1085307142
GWAS Ctlgrs1085307142
Max Magnitude0
ClinVar
Risk rs1085307142(C;C)
Alt rs1085307142(C;C)
Reference Rs1085307142(T;T)
Significance Pathogenic
Disease not provided Neuropathy
Variation info
Gene SCN11A
CLNDBN not provided Neuropathy, hereditary sensory and autonomic, type VII
Reversed 1
HGVS NC_000003.11:g.38950600A>G
CLNSRC
CLNACC RCV000488990.1, RCV000489242.1,