rs28937573

Orientation

plus

Stabilized

plus

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

Make rs28937573(C;T)

Make rs28937573(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

67165841

Gene

HSF4

is a	snp
is	mentioned by
dbSNP	rs28937573
dbSNP (classic)	rs28937573
ClinGen	rs28937573
ebi	rs28937573
HLI	rs28937573
Exac	rs28937573
Gnomad	rs28937573
Varsome	rs28937573
LitVar	rs28937573
Map	rs28937573
PheGenI	rs28937573
Biobank	rs28937573
1000 genomes	rs28937573
hgdp	rs28937573
ensembl	rs28937573
geneview	rs28937573
scholar	rs28937573
google	rs28937573
pharmgkb	rs28937573
gwascentral	rs28937573
openSNP	rs28937573
23andMe	rs28937573
SNPshot	rs28937573
SNPdbe	rs28937573
MSV3d	rs28937573
GWAS Ctlg	rs28937573

Max Magnitude

0

OMIM	602438
Desc	CATARACT, MARNER TYPE
Variant	0002
Related	also

ClinVar
Risk	rs28937573(T;T)
Alt	rs28937573(T;T)
Reference	Rs28937573(C;C)
Significance	Pathogenic
Disease	Cataract
Variation	info
Gene	HSF4
CLNDBN	Cataract, zonular
Reversed	0
HGVS	NC_000016.9:g.67199744C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007510.3,