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rs1064795711

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome3
Position38903990
GeneSCN11A
is asnp
is mentioned by
dbSNPrs1064795711
dbSNP (old)rs1064795711
ClinGenrs1064795711
ebirs1064795711
HLIrs1064795711
Exacrs1064795711
Gnomadrs1064795711
Varsomers1064795711
Maprs1064795711
PheGenIrs1064795711
Biobankrs1064795711
1000 genomesrs1064795711
hgdprs1064795711
ensemblrs1064795711
gopubmedrs1064795711
geneviewrs1064795711
scholarrs1064795711
googlers1064795711
pharmgkbrs1064795711
gwascentralrs1064795711
openSNPrs1064795711
23andMers1064795711
23andMe allrs1064795711
SNPshotrs1064795711
SNPdbers1064795711
MSV3drs1064795711
GWAS Ctlgrs1064795711
Max Magnitude0
ClinVar
Risk rs1064795711(A;A)
Alt rs1064795711(A;A)
Reference Rs1064795711(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN11A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38945481C>T
CLNSRC
CLNACC RCV000480155.1,