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rs202152511

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202152511(A;A)
Make rs202152511(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166277138
GeneLOC101929680, SCN9A
is asnp
is mentioned by
dbSNPrs202152511
dbSNP (old)rs202152511
ClinGenrs202152511
ebirs202152511
HLIrs202152511
Exacrs202152511
Gnomadrs202152511
Varsomers202152511
Maprs202152511
PheGenIrs202152511
Biobankrs202152511
1000 genomesrs202152511
hgdprs202152511
ensemblrs202152511
gopubmedrs202152511
geneviewrs202152511
scholarrs202152511
googlers202152511
pharmgkbrs202152511
gwascentralrs202152511
openSNPrs202152511
23andMers202152511
23andMe allrs202152511
SNPshotrs202152511
SNPdbers202152511
MSV3drs202152511
GWAS Ctlgrs202152511
Max Magnitude0
ClinVar
Risk rs202152511(A;A)
Alt rs202152511(A;A)
Reference Rs202152511(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101929680 SCN9A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.167133648G>A
CLNSRC
CLNACC RCV000479461.1,