rs118203966

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs118203966(A;A)

Make rs118203966(A;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

33851064

Gene

CHMP4B

is a	snp
is	mentioned by
dbSNP	rs118203966
dbSNP (classic)	rs118203966
ClinGen	rs118203966
ebi	rs118203966
HLI	rs118203966
Exac	rs118203966
Gnomad	rs118203966
Varsome	rs118203966
LitVar	rs118203966
Map	rs118203966
PheGenI	rs118203966
Biobank	rs118203966
1000 genomes	rs118203966
hgdp	rs118203966
ensembl	rs118203966
geneview	rs118203966
scholar	rs118203966
google	rs118203966
pharmgkb	rs118203966
gwascentral	rs118203966
openSNP	rs118203966
23andMe	rs118203966
SNPshot	rs118203966
SNPdbe	rs118203966
MSV3d	rs118203966
GWAS Ctlg	rs118203966

Max Magnitude

0

OMIM	610897
Desc
Variant	0002
Related	also

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 UniProtKB (protein)
CLNACC	RCV000001144.3,