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rs797044982

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGCCTC;GGCCTC) 0 common in clinvar
Make rs797044982(-;-)
Make rs797044982(-;GGCCTC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992250
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs797044982
dbSNP (old)rs797044982
ClinGenrs797044982
ebirs797044982
HLIrs797044982
Exacrs797044982
Gnomadrs797044982
Varsomers797044982
Maprs797044982
PheGenIrs797044982
Biobankrs797044982
1000 genomesrs797044982
hgdprs797044982
ensemblrs797044982
gopubmedrs797044982
geneviewrs797044982
scholarrs797044982
googlers797044982
pharmgkbrs797044982
gwascentralrs797044982
openSNPrs797044982
23andMers797044982
23andMe allrs797044982
SNP Nexus

SNPshotrs797044982
SNPdbers797044982
MSV3drs797044982
GWAS Ctlgrs797044982
Max Magnitude0
ClinVar
Risk rs797044982(-;-)
Alt rs797044982(-;-)
Reference Rs797044982(GGCCTC;GGCCTC)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848760_166848765delGAGGCC
CLNSRC
CLNACC RCV000190446.1,