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rs201659924

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201659924(C;T)
Make rs201659924(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position47607033
GeneSYN1
is asnp
is mentioned by
dbSNPrs201659924
ebirs201659924
HLIrs201659924
Exacrs201659924
Varsomers201659924
Maprs201659924
PheGenIrs201659924
hapmaprs201659924
1000 genomesrs201659924
hgdprs201659924
ensemblrs201659924
gopubmedrs201659924
geneviewrs201659924
scholarrs201659924
googlers201659924
pharmgkbrs201659924
gwascentralrs201659924
openSNPrs201659924
23andMers201659924
23andMe allrs201659924
SNP Nexus

SNPshotrs201659924
SNPdbers201659924
MSV3drs201659924
GWAS Ctlgrs201659924
Max Magnitude0
ClinVar
Risk rs201659924(T;T)
Alt rs201659924(T;T)
Reference rs201659924(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYN1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.47466432C>T
CLNSRC
CLNACC RCV000189665.2,