rs121434338

Orientation

plus

Stabilized

plus

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

Make rs121434338(A;G)

Make rs121434338(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

60822627

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs121434338
dbSNP (classic)	rs121434338
ClinGen	rs121434338
ebi	rs121434338
HLI	rs121434338
Exac	rs121434338
Gnomad	rs121434338
Varsome	rs121434338
LitVar	rs121434338
Map	rs121434338
PheGenI	rs121434338
Biobank	rs121434338
1000 genomes	rs121434338
hgdp	rs121434338
ensembl	rs121434338
geneview	rs121434338
scholar	rs121434338
google	rs121434338
pharmgkb	rs121434338
gwascentral	rs121434338
openSNP	rs121434338
23andMe	rs121434338
SNPshot	rs121434338
SNPdbe	rs121434338
MSV3d	rs121434338
GWAS Ctlg	rs121434338

Max Magnitude

0

OMIM	608892
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434338(G;G)
Alt	rs121434338(G;G)
Reference	Rs121434338(A;A)
Significance	Pathogenic
Disease	CHARGE association not provided
Variation	info
Gene	CHD7
CLNDBN	CHARGE association not provided
Reversed	0
HGVS	NC_000008.10:g.61735186A>G
CLNSRC	HGMD OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002100.4, RCV000081828.5,