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rs561449819

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs561449819(C;T)
Make rs561449819(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position46195731
GeneLSS
is asnp
is mentioned by
dbSNPrs561449819
ebirs561449819
HLIrs561449819
Exacrs561449819
Varsomers561449819
Maprs561449819
PheGenIrs561449819
hapmaprs561449819
1000 genomesrs561449819
hgdprs561449819
ensemblrs561449819
gopubmedrs561449819
geneviewrs561449819
scholarrs561449819
googlers561449819
pharmgkbrs561449819
gwascentralrs561449819
openSNPrs561449819
23andMers561449819
23andMe allrs561449819
SNP Nexus

SNPshotrs561449819
SNPdbers561449819
MSV3drs561449819
GWAS Ctlgrs561449819
Max Magnitude0
ClinVar
Risk rs561449819(T;T)
Alt rs561449819(T;T)
Reference rs561449819(C;C)
Significance Pathogenic
Disease Cataract 44
Variation info
Gene LOC101060037 LSS
CLNDBN Cataract 44
Reversed 0
HGVS NC_000021.8:g.47615645C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000206988.1,