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rs752514808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752514808(C;T)
Make rs752514808(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position135765061
GeneKCNT1
is asnp
is mentioned by
dbSNPrs752514808
dbSNP (classic)rs752514808
ClinGenrs752514808
ebirs752514808
HLIrs752514808
Exacrs752514808
Gnomadrs752514808
Varsomers752514808
LitVarrs752514808
Maprs752514808
PheGenIrs752514808
Biobankrs752514808
1000 genomesrs752514808
hgdprs752514808
ensemblrs752514808
geneviewrs752514808
scholarrs752514808
googlers752514808
pharmgkbrs752514808
gwascentralrs752514808
openSNPrs752514808
23andMers752514808
SNPshotrs752514808
SNPdbers752514808
MSV3drs752514808
GWAS Ctlgrs752514808
Max Magnitude0
ClinVar
Risk rs752514808(G;G) rs752514808(T;T)
Alt rs752514808(G;G) rs752514808(T;T)
Reference Rs752514808(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138656907C>T
CLNSRC
CLNACC RCV000420451.1,