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rs387907096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907096(C;G)
Make rs387907096(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position232522594
GenePRSS56
is asnp
is mentioned by
dbSNPrs387907096
ebirs387907096
HLIrs387907096
Exacrs387907096
Varsomers387907096
Maprs387907096
PheGenIrs387907096
hapmaprs387907096
1000 genomesrs387907096
hgdprs387907096
ensemblrs387907096
gopubmedrs387907096
geneviewrs387907096
scholarrs387907096
googlers387907096
pharmgkbrs387907096
gwascentralrs387907096
openSNPrs387907096
23andMers387907096
23andMe allrs387907096
SNP Nexus

SNPshotrs387907096
SNPdbers387907096
MSV3drs387907096
GWAS Ctlgrs387907096
Max Magnitude0
ClinVar
Risk rs387907096(G;G)
Alt rs387907096(G;G)
Reference rs387907096(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene PRSS56
CLNDBN Microphthalmia, isolated 6
Reversed 0
HGVS NC_000002.11:g.233387304C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024076.4,