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rs757027813

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757027813(G;T)
Make rs757027813(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position47575169
GeneSYN1
is asnp
is mentioned by
dbSNPrs757027813
ebirs757027813
HLIrs757027813
Exacrs757027813
Varsomers757027813
Maprs757027813
PheGenIrs757027813
hapmaprs757027813
1000 genomesrs757027813
hgdprs757027813
ensemblrs757027813
gopubmedrs757027813
geneviewrs757027813
scholarrs757027813
googlers757027813
pharmgkbrs757027813
gwascentralrs757027813
openSNPrs757027813
23andMers757027813
23andMe allrs757027813
SNP Nexus

SNPshotrs757027813
SNPdbers757027813
MSV3drs757027813
GWAS Ctlgrs757027813
Max Magnitude0
ClinVar
Risk rs757027813(A,T;A,T)
Alt rs757027813(A,T;A,T)
Reference rs757027813(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SYN1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.47434568G>A
CLNSRC
CLNACC RCV000189652.1,