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rs139969658

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139969658(C;T)
Make rs139969658(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7585738
GeneDSP
is asnp
is mentioned by
dbSNPrs139969658
ebirs139969658
HLIrs139969658
Exacrs139969658
Varsomers139969658
Maprs139969658
PheGenIrs139969658
hapmaprs139969658
1000 genomesrs139969658
hgdprs139969658
ensemblrs139969658
gopubmedrs139969658
geneviewrs139969658
scholarrs139969658
googlers139969658
pharmgkbrs139969658
gwascentralrs139969658
openSNPrs139969658
23andMers139969658
23andMe allrs139969658
SNP Nexus

SNPshotrs139969658
SNPdbers139969658
MSV3drs139969658
GWAS Ctlgrs139969658
Max Magnitude0
ClinVar
Risk rs139969658(T;T)
Alt rs139969658(T;T)
Reference rs139969658(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7585971C>T
CLNSRC
CLNACC RCV000181351.2,