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rs1057524752

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524752(A;T)
Make rs1057524752(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166047728
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057524752
dbSNP (old)rs1057524752
ClinGenrs1057524752
ebirs1057524752
HLIrs1057524752
Exacrs1057524752
Gnomadrs1057524752
Varsomers1057524752
Maprs1057524752
PheGenIrs1057524752
Biobankrs1057524752
1000 genomesrs1057524752
hgdprs1057524752
ensemblrs1057524752
gopubmedrs1057524752
geneviewrs1057524752
scholarrs1057524752
googlers1057524752
pharmgkbrs1057524752
gwascentralrs1057524752
openSNPrs1057524752
23andMers1057524752
23andMe allrs1057524752
SNPshotrs1057524752
SNPdbers1057524752
MSV3drs1057524752
GWAS Ctlgrs1057524752
Max Magnitude0
ClinVar
Risk rs1057524752(T;T)
Alt rs1057524752(T;T)
Reference Rs1057524752(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904238T>A
CLNSRC
CLNACC RCV000443388.1,