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rs730882159

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882159(-;-)
Make rs730882159(-;G)
Make rs730882159(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position232523186
GenePRSS56
is asnp
is mentioned by
dbSNPrs730882159
ebirs730882159
HLIrs730882159
Exacrs730882159
Varsomers730882159
Maprs730882159
PheGenIrs730882159
hapmaprs730882159
1000 genomesrs730882159
hgdprs730882159
ensemblrs730882159
gopubmedrs730882159
geneviewrs730882159
scholarrs730882159
googlers730882159
pharmgkbrs730882159
gwascentralrs730882159
openSNPrs730882159
23andMers730882159
23andMe allrs730882159
SNP Nexus

SNPshotrs730882159
SNPdbers730882159
MSV3drs730882159
GWAS Ctlgrs730882159
Max Magnitude0
ClinVar
Risk rs730882159(G;G)
Alt rs730882159(G;G)
Reference rs730882159(;)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene PRSS56
CLNDBN Microphthalmia, isolated 6
Reversed 0
HGVS NC_000002.11:g.233387896dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000162040.3,