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rs786205222

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205222(A;C)
Make rs786205222(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position79598995
GeneLOC101928230, MAF
is asnp
is mentioned by
dbSNPrs786205222
ebirs786205222
HLIrs786205222
Exacrs786205222
Varsomers786205222
Maprs786205222
PheGenIrs786205222
hapmaprs786205222
1000 genomesrs786205222
hgdprs786205222
ensemblrs786205222
gopubmedrs786205222
geneviewrs786205222
scholarrs786205222
googlers786205222
pharmgkbrs786205222
gwascentralrs786205222
openSNPrs786205222
23andMers786205222
23andMe allrs786205222
SNP Nexus

SNPshotrs786205222
SNPdbers786205222
MSV3drs786205222
GWAS Ctlgrs786205222
Max Magnitude0
ClinVar
Risk rs786205222(C;C)
Alt rs786205222(C;C)
Reference rs786205222(A;A)
Significance Pathogenic
Disease Cataract
Variation info
Gene MAF LOC101928230
CLNDBN Cataract, pulverulent, juvenile-onset
Reversed 1
HGVS NC_000016.9:g.79632892T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000170459.4,