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rs864622780

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622780(C;C)
Make rs864622780(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position46195752
GeneLSS
is asnp
is mentioned by
dbSNPrs864622780
ebirs864622780
HLIrs864622780
Exacrs864622780
Varsomers864622780
Maprs864622780
PheGenIrs864622780
hapmaprs864622780
1000 genomesrs864622780
hgdprs864622780
ensemblrs864622780
gopubmedrs864622780
geneviewrs864622780
scholarrs864622780
googlers864622780
pharmgkbrs864622780
gwascentralrs864622780
openSNPrs864622780
23andMers864622780
23andMe allrs864622780
SNP Nexus

SNPshotrs864622780
SNPdbers864622780
MSV3drs864622780
GWAS Ctlgrs864622780
Max Magnitude0
ClinVar
Risk rs864622780(C;C)
Alt rs864622780(C;C)
Reference rs864622780(T;T)
Significance Pathogenic
Disease Cataract 44
Variation info
Gene LOC101060037 LSS
CLNDBN Cataract 44
Reversed 1
HGVS NC_000021.8:g.47615666A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000207005.1,