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rs879254102

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879254102(A;A)
Make rs879254102(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position166277257
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs879254102
dbSNP (classic)rs879254102
ClinGenrs879254102
ebirs879254102
HLIrs879254102
Exacrs879254102
Gnomadrs879254102
Varsomers879254102
LitVarrs879254102
Maprs879254102
PheGenIrs879254102
Biobankrs879254102
1000 genomesrs879254102
hgdprs879254102
ensemblrs879254102
geneviewrs879254102
scholarrs879254102
googlers879254102
pharmgkbrs879254102
gwascentralrs879254102
openSNPrs879254102
23andMers879254102
SNPshotrs879254102
SNPdbers879254102
MSV3drs879254102
GWAS Ctlgrs879254102
Max Magnitude0
ClinVar
Risk rs879254102(A;A)
Alt rs879254102(A;A)
Reference Rs879254102(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101929680 SCN9A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.167133767C>T
CLNSRC
CLNACC RCV000236068.1,