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rs6050307

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6050307(G;T)
Make rs6050307(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position25081706
GeneVSX1
is asnp
is mentioned by
dbSNPrs6050307
dbSNP (old)rs6050307
ClinGenrs6050307
ebirs6050307
HLIrs6050307
Exacrs6050307
Varsomers6050307
Maprs6050307
PheGenIrs6050307
Biobankrs6050307
1000 genomesrs6050307
hgdprs6050307
ensemblrs6050307
gopubmedrs6050307
geneviewrs6050307
scholarrs6050307
googlers6050307
pharmgkbrs6050307
gwascentralrs6050307
openSNPrs6050307
23andMers6050307
23andMe allrs6050307
SNP Nexus

SNPshotrs6050307
SNPdbers6050307
MSV3drs6050307
GWAS Ctlgrs6050307
Max Magnitude0

[PMID 25675348] Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population

ClinVar
Risk rs6050307(T;T)
Alt rs6050307(T;T)
Reference Rs6050307(G;G)
Significance Non-pathogenic
Disease Posterior Polymorphous Corneal Dystrophy
Variation info
Gene VSX1
CLNDBN Posterior Polymorphous Corneal Dystrophy
Reversed 0
HGVS NC_000020.10:g.25062342G>T
CLNSRC
CLNACC RCV000260491.1,