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rs200972952

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200972952(A;A)
Make rs200972952(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166306951
GeneSCN9A
is asnp
is mentioned by
dbSNPrs200972952
dbSNP (classic)rs200972952
ClinGenrs200972952
ebirs200972952
HLIrs200972952
Exacrs200972952
Gnomadrs200972952
Varsomers200972952
LitVarrs200972952
Maprs200972952
PheGenIrs200972952
Biobankrs200972952
1000 genomesrs200972952
hgdprs200972952
ensemblrs200972952
geneviewrs200972952
scholarrs200972952
googlers200972952
pharmgkbrs200972952
gwascentralrs200972952
openSNPrs200972952
23andMers200972952
23andMe allrs200972952
SNPshotrs200972952
SNPdbers200972952
MSV3drs200972952
GWAS Ctlgrs200972952
Max Magnitude0
ClinVar
Risk rs200972952(A;A) rs200972952(T;T)
Alt rs200972952(A;A) rs200972952(T;T)
Reference Rs200972952(G;G)
Significance Pathogenic
Disease Pain insensitivity
Variation info
Gene SCN9A
CLNDBN Pain insensitivity
Reversed 0
HGVS NC_000002.11:g.167163461G>A
CLNSRC
CLNACC RCV000415348.1,