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rs143549737

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs143549737(G;G)
Make rs143549737(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position107459011
GenePDSS2
is asnp
is mentioned by
dbSNPrs143549737
ebirs143549737
HLIrs143549737
Exacrs143549737
Varsomers143549737
Maprs143549737
PheGenIrs143549737
hapmaprs143549737
1000 genomesrs143549737
hgdprs143549737
ensemblrs143549737
gopubmedrs143549737
geneviewrs143549737
scholarrs143549737
googlers143549737
pharmgkbrs143549737
gwascentralrs143549737
openSNPrs143549737
23andMers143549737
23andMe allrs143549737
SNP Nexus

SNPshotrs143549737
SNPdbers143549737
MSV3drs143549737
GWAS Ctlgrs143549737
Max Magnitude0
ClinVar
Risk rs143549737(G;G)
Alt rs143549737(G;G)
Reference rs143549737(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDSS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.107780215T>G
CLNSRC
CLNACC RCV000199611.1,