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rs876661206

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661206(A;T)
Make rs876661206(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position166204222
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs876661206
ebirs876661206
HLIrs876661206
Exacrs876661206
Varsomers876661206
Maprs876661206
PheGenIrs876661206
hapmaprs876661206
1000 genomesrs876661206
hgdprs876661206
ensemblrs876661206
gopubmedrs876661206
geneviewrs876661206
scholarrs876661206
googlers876661206
pharmgkbrs876661206
gwascentralrs876661206
openSNPrs876661206
23andMers876661206
23andMe allrs876661206
SNP Nexus

SNPshotrs876661206
SNPdbers876661206
MSV3drs876661206
GWAS Ctlgrs876661206
Max Magnitude0
ClinVar
Risk rs876661206(T;T)
Alt rs876661206(T;T)
Reference rs876661206(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101929680 SCN9A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.167060732T>A
CLNSRC
CLNACC RCV000220058.1,