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rs876657372

From SNPedia

Orientationminus
Geno Mag Summary
(ACGT;ACGT) 0 common in clinvar
Make rs876657372(-;-)
Make rs876657372(-;ACGT)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position118313332
GenePRSS12
is asnp
is mentioned by
dbSNPrs876657372
ebirs876657372
HLIrs876657372
Exacrs876657372
Varsomers876657372
Maprs876657372
PheGenIrs876657372
hapmaprs876657372
1000 genomesrs876657372
hgdprs876657372
ensemblrs876657372
gopubmedrs876657372
geneviewrs876657372
scholarrs876657372
googlers876657372
pharmgkbrs876657372
gwascentralrs876657372
openSNPrs876657372
23andMers876657372
23andMe allrs876657372
SNP Nexus

SNPshotrs876657372
SNPdbers876657372
MSV3drs876657372
GWAS Ctlgrs876657372
Max Magnitude0
ClinVar
Risk rs876657372(;)
Alt rs876657372(;)
Reference rs876657372(ACGT;ACGT)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene PRSS12
CLNDBN Mental retardation, autosomal recessive 1
Reversed 1
HGVS NC_000004.11:g.119234487_119234490delACGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000004317.3,