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rs74703359

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74703359(G;T)
Make rs74703359(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position232523470
GenePRSS56
is asnp
is mentioned by
dbSNPrs74703359
ebirs74703359
HLIrs74703359
Exacrs74703359
Varsomers74703359
Maprs74703359
PheGenIrs74703359
hapmaprs74703359
1000 genomesrs74703359
hgdprs74703359
ensemblrs74703359
gopubmedrs74703359
geneviewrs74703359
scholarrs74703359
googlers74703359
pharmgkbrs74703359
gwascentralrs74703359
openSNPrs74703359
23andMers74703359
23andMe allrs74703359
SNP Nexus

SNPshotrs74703359
SNPdbers74703359
MSV3drs74703359
GWAS Ctlgrs74703359
Max Magnitude0
ClinVar
Risk rs74703359(T;T)
Alt rs74703359(T;T)
Reference rs74703359(G;G)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene PRSS56
CLNDBN Microphthalmia, isolated 6
Reversed 0
HGVS NC_000002.11:g.233388180G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000162039.3,