rs121909049

Orientation

plus

Stabilized

plus

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

Make rs121909049(A;A)

Make rs121909049(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

67164867

Gene

HSF4

is a	snp
is	mentioned by
dbSNP	rs121909049
dbSNP (classic)	rs121909049
ClinGen	rs121909049
ebi	rs121909049
HLI	rs121909049
Exac	rs121909049
Gnomad	rs121909049
Varsome	rs121909049
LitVar	rs121909049
Map	rs121909049
PheGenI	rs121909049
Biobank	rs121909049
1000 genomes	rs121909049
hgdp	rs121909049
ensembl	rs121909049
geneview	rs121909049
scholar	rs121909049
google	rs121909049
pharmgkb	rs121909049
gwascentral	rs121909049
openSNP	rs121909049
23andMe	rs121909049
SNPshot	rs121909049
SNPdbe	rs121909049
MSV3d	rs121909049
GWAS Ctlg	rs121909049

Max Magnitude

0

OMIM	602438
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909049(A;A)
Alt	rs121909049(A;A)
Reference	Rs121909049(C;C)
Significance	Pathogenic
Disease	Cataract
Variation	info
Gene	HSF4
CLNDBN	Cataract, zonular
Reversed	0
HGVS	NC_000016.9:g.67198770C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007511.3,