Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518162(A;A)
Make rs1057518162(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166280559
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs1057518162
dbSNP (old)rs1057518162
ClinGenrs1057518162
ebirs1057518162
HLIrs1057518162
Exacrs1057518162
Gnomadrs1057518162
Varsomers1057518162
LitVarrs1057518162
Maprs1057518162
PheGenIrs1057518162
Biobankrs1057518162
1000 genomesrs1057518162
hgdprs1057518162
ensemblrs1057518162
gopubmedrs1057518162
geneviewrs1057518162
scholarrs1057518162
googlers1057518162
pharmgkbrs1057518162
gwascentralrs1057518162
openSNPrs1057518162
23andMers1057518162
23andMe allrs1057518162
SNPshotrs1057518162
SNPdbers1057518162
MSV3drs1057518162
GWAS Ctlgrs1057518162
Max Magnitude0
ClinVar
Risk rs1057518162(A;A)
Alt rs1057518162(A;A)
Reference Rs1057518162(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC101929680 SCN9A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.167137069C>T
CLNSRC
CLNACC RCV000414021.1,