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rs746241591

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746241591(A;A)
Make rs746241591(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position166204359
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs746241591
ebirs746241591
HLIrs746241591
Exacrs746241591
Varsomers746241591
Maprs746241591
PheGenIrs746241591
hapmaprs746241591
1000 genomesrs746241591
hgdprs746241591
ensemblrs746241591
gopubmedrs746241591
geneviewrs746241591
scholarrs746241591
googlers746241591
pharmgkbrs746241591
gwascentralrs746241591
openSNPrs746241591
23andMers746241591
23andMe allrs746241591
SNP Nexus

SNPshotrs746241591
SNPdbers746241591
MSV3drs746241591
GWAS Ctlgrs746241591
Max Magnitude0
ClinVar
Risk rs746241591(A;A)
Alt rs746241591(A;A)
Reference rs746241591(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC101929680 SCN9A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.167060869C>A
CLNSRC
CLNACC RCV000236300.1,