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rs770416478

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770416478(C;G)
Make rs770416478(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position166199247
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs770416478
ebirs770416478
HLIrs770416478
Exacrs770416478
Varsomers770416478
Maprs770416478
PheGenIrs770416478
hapmaprs770416478
1000 genomesrs770416478
hgdprs770416478
ensemblrs770416478
gopubmedrs770416478
geneviewrs770416478
scholarrs770416478
googlers770416478
pharmgkbrs770416478
gwascentralrs770416478
openSNPrs770416478
23andMers770416478
23andMe allrs770416478
SNP Nexus

SNPshotrs770416478
SNPdbers770416478
MSV3drs770416478
GWAS Ctlgrs770416478
Max Magnitude0
ClinVar
Risk rs770416478(G;G)
Alt rs770416478(G;G)
Reference rs770416478(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101929680 SCN9A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.167055757C>A
CLNSRC
CLNACC RCV000236372.1,