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rs786205635

From SNPedia

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Geno Mag Summary
(CTTA;CTTA) 0 common in clinvar
Make rs786205635(-;-)
Make rs786205635(-;CTTA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165323158
GeneSCN2A
is asnp
is mentioned by
dbSNPrs786205635
ebirs786205635
HLIrs786205635
Exacrs786205635
Varsomers786205635
Maprs786205635
PheGenIrs786205635
hapmaprs786205635
1000 genomesrs786205635
hgdprs786205635
ensemblrs786205635
gopubmedrs786205635
geneviewrs786205635
scholarrs786205635
googlers786205635
pharmgkbrs786205635
gwascentralrs786205635
openSNPrs786205635
23andMers786205635
23andMe allrs786205635
SNP Nexus

SNPshotrs786205635
SNPdbers786205635
MSV3drs786205635
GWAS Ctlgrs786205635
Max Magnitude0
ClinVar
Risk rs786205635(;)
Alt rs786205635(;)
Reference rs786205635(CTTA;CTTA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166179668_166179671delCTTA
CLNSRC
CLNACC RCV000171497.1,