rs1057518576

Orientation

plus

Stabilized

plus

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

Make rs1057518576(GCTACAAGAAACAC;T)

Make rs1057518576(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60845376

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057518576
dbSNP (classic)	rs1057518576
ClinGen	rs1057518576
ebi	rs1057518576
HLI	rs1057518576
Exac	rs1057518576
Gnomad	rs1057518576
Varsome	rs1057518576
LitVar	rs1057518576
Map	rs1057518576
PheGenI	rs1057518576
Biobank	rs1057518576
1000 genomes	rs1057518576
hgdp	rs1057518576
ensembl	rs1057518576
geneview	rs1057518576
scholar	rs1057518576
google	rs1057518576
pharmgkb	rs1057518576
gwascentral	rs1057518576
openSNP	rs1057518576
23andMe	rs1057518576
SNPshot	rs1057518576
SNPdbe	rs1057518576
MSV3d	rs1057518576
GWAS Ctlg	rs1057518576

Max Magnitude

0

ClinVar
Risk	rs1057518576(T;T)
Alt	rs1057518576(T;T)
Reference	Rs1057518576(GCTACAAGAAACAC;GCTACAAGAAACAC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61757935_61757948delGCTACAAGAAACACinsT
CLNSRC
CLNACC	RCV000413631.1,