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rs71428908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs71428908(C;C)
Make rs71428908(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position166304242
GeneSCN9A
is asnp
is mentioned by
dbSNPrs71428908
dbSNP (classic)rs71428908
ClinGenrs71428908
ebirs71428908
HLIrs71428908
Exacrs71428908
Gnomadrs71428908
Varsomers71428908
LitVarrs71428908
Maprs71428908
PheGenIrs71428908
Biobankrs71428908
1000 genomesrs71428908
hgdprs71428908
ensemblrs71428908
geneviewrs71428908
scholarrs71428908
googlers71428908
pharmgkbrs71428908
gwascentralrs71428908
openSNPrs71428908
23andMers71428908
23andMe allrs71428908
SNPshotrs71428908
SNPdbers71428908
MSV3drs71428908
GWAS Ctlgrs71428908
Max Magnitude0
ClinVar
Risk rs71428908(A;A) rs71428908(C;C)
Alt rs71428908(A;A) rs71428908(C;C)
Reference Rs71428908(G;G)
Significance Other
Disease not provided not specified
Variation info
Gene SCN9A
CLNDBN not provided not specified
Reversed 0
HGVS NC_000002.11:g.167160752G>C
CLNSRC UniProtKB (protein)
CLNACC RCV000179414.3, RCV000192901.2,