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rs369804864

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369804864(A;A)
Make rs369804864(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11577187
GeneACP5, ZNF627
is asnp
is mentioned by
dbSNPrs369804864
ebirs369804864
HLIrs369804864
Exacrs369804864
Varsomers369804864
Maprs369804864
PheGenIrs369804864
hapmaprs369804864
1000 genomesrs369804864
hgdprs369804864
ensemblrs369804864
gopubmedrs369804864
geneviewrs369804864
scholarrs369804864
googlers369804864
pharmgkbrs369804864
gwascentralrs369804864
openSNPrs369804864
23andMers369804864
23andMe allrs369804864
SNP Nexus

SNPshotrs369804864
SNPdbers369804864
MSV3drs369804864
GWAS Ctlgrs369804864
Max Magnitude0
ClinVar
Risk rs369804864(A;A)
Alt rs369804864(A;A)
Reference rs369804864(G;G)
Significance Pathogenic
Disease Spondyloenchondrodysplasia with immune dysregulation
Variation info
Gene ACP5
CLNDBN Spondyloenchondrodysplasia with immune dysregulation
Reversed 0
HGVS NC_000019.9:g.11688002G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210945.1,