Have questions? Visit https://www.reddit.com/r/SNPedia

rs756898971

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756898971(C;T)
Make rs756898971(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38192203
GeneSIPA1L3
is asnp
is mentioned by
dbSNPrs756898971
ebirs756898971
HLIrs756898971
Exacrs756898971
Varsomers756898971
Maprs756898971
PheGenIrs756898971
hapmaprs756898971
1000 genomesrs756898971
hgdprs756898971
ensemblrs756898971
gopubmedrs756898971
geneviewrs756898971
scholarrs756898971
googlers756898971
pharmgkbrs756898971
gwascentralrs756898971
openSNPrs756898971
23andMers756898971
23andMe allrs756898971
SNP Nexus

SNPshotrs756898971
SNPdbers756898971
MSV3drs756898971
GWAS Ctlgrs756898971
Max Magnitude0
ClinVar
Risk rs756898971(T;T)
Alt rs756898971(T;T)
Reference rs756898971(C;C)
Significance Pathogenic
Disease Cataract 45
Variation info
Gene SIPA1L3
CLNDBN Cataract 45
Reversed 0
HGVS NC_000019.9:g.38682843C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000208874.1,