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rs1057521746

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521746(A;A)
Make rs1057521746(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166009753
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1057521746
dbSNP (classic)rs1057521746
ClinGenrs1057521746
ebirs1057521746
HLIrs1057521746
Exacrs1057521746
Gnomadrs1057521746
Varsomers1057521746
LitVarrs1057521746
Maprs1057521746
PheGenIrs1057521746
Biobankrs1057521746
1000 genomesrs1057521746
hgdprs1057521746
ensemblrs1057521746
geneviewrs1057521746
scholarrs1057521746
googlers1057521746
pharmgkbrs1057521746
gwascentralrs1057521746
openSNPrs1057521746
23andMers1057521746
SNPshotrs1057521746
SNPdbers1057521746
MSV3drs1057521746
GWAS Ctlgrs1057521746
Max Magnitude0
ClinVar
Risk rs1057521746(A;A)
Alt rs1057521746(A;A)
Reference Rs1057521746(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166866263G>T
CLNSRC
CLNACC RCV000430833.1,