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

rs104893685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893685(C;T)
Make rs104893685(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position133450432
GeneBFSP2, BFSP2-AS1
is asnp
is mentioned by
dbSNPrs104893685
ebirs104893685
HLIrs104893685
Exacrs104893685
Varsomers104893685
Maprs104893685
PheGenIrs104893685
hapmaprs104893685
1000 genomesrs104893685
hgdprs104893685
ensemblrs104893685
gopubmedrs104893685
geneviewrs104893685
scholarrs104893685
googlers104893685
pharmgkbrs104893685
gwascentralrs104893685
openSNPrs104893685
23andMers104893685
23andMe allrs104893685
SNP Nexus

SNPshotrs104893685
SNPdbers104893685
MSV3drs104893685
GWAS Ctlgrs104893685
Max Magnitude0
OMIM603212
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893685(A,T;A,T)
Alt rs104893685(A,T;A,T)
Reference rs104893685(C;C)
Significance Pathogenic
Disease Cataract not provided
Variation info
Gene BFSP2-AS1 BFSP2
CLNDBN Cataract, autosomal dominant, multiple types 1 not provided
Reversed 0
HGVS NC_000003.11:g.133169276C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006961.3, RCV000056969.1,