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rs770528538

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770528538(A;A)
Make rs770528538(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position126338400
GeneDCPS
is asnp
is mentioned by
dbSNPrs770528538
dbSNP (classic)rs770528538
ClinGenrs770528538
ebirs770528538
HLIrs770528538
Exacrs770528538
Gnomadrs770528538
Varsomers770528538
LitVarrs770528538
Maprs770528538
PheGenIrs770528538
Biobankrs770528538
1000 genomesrs770528538
hgdprs770528538
ensemblrs770528538
geneviewrs770528538
scholarrs770528538
googlers770528538
pharmgkbrs770528538
gwascentralrs770528538
openSNPrs770528538
23andMers770528538
SNPshotrs770528538
SNPdbers770528538
MSV3drs770528538
GWAS Ctlgrs770528538
Max Magnitude0
ClinVar
Risk rs770528538(A;A) rs770528538(T;T)
Alt rs770528538(A;A) rs770528538(T;T)
Reference Rs770528538(G;G)
Significance Pathogenic
Disease AL-RAQAD SYNDROME
Variation info
Gene DCPS
CLNDBN AL-RAQAD SYNDROME
Reversed 0
HGVS NC_000011.9:g.126208295G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000412559.1,