rs1004428835

Orientation

plus

Stabilized

plus

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

Make rs1004428835(C;T)

Make rs1004428835(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

88427489

Gene

ZNF469

is a	snp
is	mentioned by
dbSNP	rs1004428835
dbSNP (classic)	rs1004428835
ClinGen	rs1004428835
ebi	rs1004428835
HLI	rs1004428835
Exac	rs1004428835
Gnomad	rs1004428835
Varsome	rs1004428835
LitVar	rs1004428835
Map	rs1004428835
PheGenI	rs1004428835
Biobank	rs1004428835
1000 genomes	rs1004428835
hgdp	rs1004428835
ensembl	rs1004428835
geneview	rs1004428835
scholar	rs1004428835
google	rs1004428835
pharmgkb	rs1004428835
gwascentral	rs1004428835
openSNP	rs1004428835
23andMe	rs1004428835
SNPshot	rs1004428835
SNPdbe	rs1004428835
MSV3d	rs1004428835
GWAS Ctlg	rs1004428835

Max Magnitude

0

ClinVar
Risk	rs1004428835(T;T)
Alt	rs1004428835(T;T)
Reference	Rs1004428835(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ZNF469
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.88493897C>T
CLNSRC
CLNACC	RCV000443600.1,