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rs200979563

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200979563(A;A)
Make rs200979563(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position31001159
GeneSTX1B
is asnp
is mentioned by
dbSNPrs200979563
ebirs200979563
HLIrs200979563
Exacrs200979563
Varsomers200979563
Maprs200979563
PheGenIrs200979563
hapmaprs200979563
1000 genomesrs200979563
hgdprs200979563
ensemblrs200979563
gopubmedrs200979563
geneviewrs200979563
scholarrs200979563
googlers200979563
pharmgkbrs200979563
gwascentralrs200979563
openSNPrs200979563
23andMers200979563
23andMe allrs200979563
SNP Nexus

SNPshotrs200979563
SNPdbers200979563
MSV3drs200979563
GWAS Ctlgrs200979563
Max Magnitude0
ClinVar
Risk rs200979563(A,T;A,T)
Alt rs200979563(A,T;A,T)
Reference rs200979563(G;G)
Significance Pathogenic
Disease Generalized epilepsy with febrile seizures plus
Variation info
Gene STX1B
CLNDBN Generalized epilepsy with febrile seizures plus, type 9
Reversed 0
HGVS NC_000016.9:g.31012480G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149792.3,