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rs118203966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203966(A;A)
Make rs118203966(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position33851064
GeneCHMP4B
is asnp
is mentioned by
dbSNPrs118203966
ebirs118203966
HLIrs118203966
Exacrs118203966
Varsomers118203966
Maprs118203966
PheGenIrs118203966
hapmaprs118203966
1000 genomesrs118203966
hgdprs118203966
ensemblrs118203966
gopubmedrs118203966
geneviewrs118203966
scholarrs118203966
googlers118203966
pharmgkbrs118203966
gwascentralrs118203966
openSNPrs118203966
23andMers118203966
23andMe allrs118203966
SNP Nexus

SNPshotrs118203966
SNPdbers118203966
MSV3drs118203966
GWAS Ctlgrs118203966
Max Magnitude0
OMIM610897
Desc
Variant0002
Relatedalso
ClinVar
Risk rs118203966(A;A)
Alt rs118203966(A;A)
Reference rs118203966(G;G)
Significance Pathogenic
Disease Cataract
Variation info
Gene CHMP4B
CLNDBN Cataract, posterior polar, 3
Reversed 0
HGVS NC_000020.10:g.32438870G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001144.3,