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rs1057521718

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521718(A;G)
Make rs1057521718(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position96287126
GenePTDSS1
is asnp
is mentioned by
dbSNPrs1057521718
dbSNP (classic)rs1057521718
ClinGenrs1057521718
ebirs1057521718
HLIrs1057521718
Exacrs1057521718
Gnomadrs1057521718
Varsomers1057521718
LitVarrs1057521718
Maprs1057521718
PheGenIrs1057521718
Biobankrs1057521718
1000 genomesrs1057521718
hgdprs1057521718
ensemblrs1057521718
geneviewrs1057521718
scholarrs1057521718
googlers1057521718
pharmgkbrs1057521718
gwascentralrs1057521718
openSNPrs1057521718
23andMers1057521718
SNPshotrs1057521718
SNPdbers1057521718
MSV3drs1057521718
GWAS Ctlgrs1057521718
Max Magnitude0
ClinVar
Risk rs1057521718(G;G)
Alt rs1057521718(G;G)
Reference Rs1057521718(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTDSS1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.97299354A>G
CLNSRC
CLNACC RCV000443001.1,