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rs1085307542

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position165388662
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1085307542
dbSNP (old)rs1085307542
ClinGenrs1085307542
ebirs1085307542
HLIrs1085307542
Exacrs1085307542
Gnomadrs1085307542
Varsomers1085307542
LitVarrs1085307542
Maprs1085307542
PheGenIrs1085307542
Biobankrs1085307542
1000 genomesrs1085307542
hgdprs1085307542
ensemblrs1085307542
gopubmedrs1085307542
geneviewrs1085307542
scholarrs1085307542
googlers1085307542
pharmgkbrs1085307542
gwascentralrs1085307542
openSNPrs1085307542
23andMers1085307542
23andMe allrs1085307542
SNPshotrs1085307542
SNPdbers1085307542
MSV3drs1085307542
GWAS Ctlgrs1085307542
Max Magnitude0
ClinVar
Risk rs1085307542(C;C)
Alt rs1085307542(C;C)
Reference Rs1085307542(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245172T>C
CLNSRC
CLNACC RCV000490238.1,