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rs864309678

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309678(C;C)
Make rs864309678(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position79599084
GeneLOC101928230, MAF
is asnp
is mentioned by
dbSNPrs864309678
ebirs864309678
HLIrs864309678
Exacrs864309678
Varsomers864309678
Maprs864309678
PheGenIrs864309678
hapmaprs864309678
1000 genomesrs864309678
hgdprs864309678
ensemblrs864309678
gopubmedrs864309678
geneviewrs864309678
scholarrs864309678
googlers864309678
pharmgkbrs864309678
gwascentralrs864309678
openSNPrs864309678
23andMers864309678
23andMe allrs864309678
SNP Nexus

SNPshotrs864309678
SNPdbers864309678
MSV3drs864309678
GWAS Ctlgrs864309678
Max Magnitude0
ClinVar
Risk rs864309678(C;C)
Alt rs864309678(C;C)
Reference rs864309678(G;G)
Significance Probable-Pathogenic
Disease Congenital cataract
Variation info
Gene MAF LOC101928230
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000016.9:g.79632981C>G
CLNSRC
CLNACC RCV000203389.1,