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rs797044981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTCTTGGCC;GTCTTGGCC) 0 common in clinvar
Make rs797044981(-;-)
Make rs797044981(-;GTCTTGGCC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166038028
GeneSCN1A
is asnp
is mentioned by
dbSNPrs797044981
dbSNP (old)rs797044981
ClinGenrs797044981
ebirs797044981
HLIrs797044981
Exacrs797044981
Gnomadrs797044981
Varsomers797044981
Maprs797044981
PheGenIrs797044981
Biobankrs797044981
1000 genomesrs797044981
hgdprs797044981
ensemblrs797044981
gopubmedrs797044981
geneviewrs797044981
scholarrs797044981
googlers797044981
pharmgkbrs797044981
gwascentralrs797044981
openSNPrs797044981
23andMers797044981
23andMe allrs797044981
SNP Nexus

SNPshotrs797044981
SNPdbers797044981
MSV3drs797044981
GWAS Ctlgrs797044981
Max Magnitude0
ClinVar
Risk rs797044981(-;-)
Alt rs797044981(-;-)
Reference Rs797044981(GTCTTGGCC;GTCTTGGCC)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894538_166894546delGGCCAAGAC
CLNSRC
CLNACC RCV000190445.1,