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rs786205598

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205598(C;T)
Make rs786205598(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127668159
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs786205598
ebirs786205598
HLIrs786205598
Exacrs786205598
Varsomers786205598
Maprs786205598
PheGenIrs786205598
hapmaprs786205598
1000 genomesrs786205598
hgdprs786205598
ensemblrs786205598
gopubmedrs786205598
geneviewrs786205598
scholarrs786205598
googlers786205598
pharmgkbrs786205598
gwascentralrs786205598
openSNPrs786205598
23andMers786205598
23andMe allrs786205598
SNP Nexus

SNPshotrs786205598
SNPdbers786205598
MSV3drs786205598
GWAS Ctlgrs786205598
Max Magnitude0
ClinVar
Risk rs786205598(T;T)
Alt rs786205598(T;T)
Reference rs786205598(C;C)
Significance Other
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130430438C>T
CLNSRC
CLNACC RCV000171427.3,