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rs1057518900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518900(C;T)
Make rs1057518900(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166284785
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs1057518900
dbSNP (classic)rs1057518900
ClinGenrs1057518900
ebirs1057518900
HLIrs1057518900
Exacrs1057518900
Gnomadrs1057518900
Varsomers1057518900
LitVarrs1057518900
Maprs1057518900
PheGenIrs1057518900
Biobankrs1057518900
1000 genomesrs1057518900
hgdprs1057518900
ensemblrs1057518900
geneviewrs1057518900
scholarrs1057518900
googlers1057518900
pharmgkbrs1057518900
gwascentralrs1057518900
openSNPrs1057518900
23andMers1057518900
23andMe allrs1057518900
SNPshotrs1057518900
SNPdbers1057518900
MSV3drs1057518900
GWAS Ctlgrs1057518900
Max Magnitude0
ClinVar
Risk rs1057518900(T;T)
Alt rs1057518900(T;T)
Reference Rs1057518900(C;C)
Significance Pathogenic
Disease Pain insensitivity
Variation info
Gene LOC101929680 SCN9A
CLNDBN Pain insensitivity
Reversed 1
HGVS NC_000002.11:g.167141295G>A
CLNSRC
CLNACC RCV000414858.1,