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rs796052668

From SNPedia

Orientationminus
Make rs796052668(-;-)
Make rs796052668(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63407375
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052668
ebirs796052668
HLIrs796052668
Exacrs796052668
Varsomers796052668
Maprs796052668
PheGenIrs796052668
hapmaprs796052668
1000 genomesrs796052668
hgdprs796052668
ensemblrs796052668
gopubmedrs796052668
geneviewrs796052668
scholarrs796052668
googlers796052668
pharmgkbrs796052668
gwascentralrs796052668
openSNPrs796052668
23andMers796052668
23andMe allrs796052668
SNP Nexus

SNPshotrs796052668
SNPdbers796052668
MSV3drs796052668
GWAS Ctlgrs796052668
Max Magnitude
ClinVar
Risk rs796052668(;)
Alt rs796052668(;)
Reference rs796052668(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62038728delC
CLNSRC
CLNACC RCV000187950.1,