rs1060499547

Orientation

plus

Stabilized

plus

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

Make rs1060499547(A;G)

Make rs1060499547(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

130862890

Gene

ABL1

is a	snp
is	mentioned by
dbSNP	rs1060499547
dbSNP (classic)	rs1060499547
ClinGen	rs1060499547
ebi	rs1060499547
HLI	rs1060499547
Exac	rs1060499547
Gnomad	rs1060499547
Varsome	rs1060499547
LitVar	rs1060499547
Map	rs1060499547
PheGenI	rs1060499547
Biobank	rs1060499547
1000 genomes	rs1060499547
hgdp	rs1060499547
ensembl	rs1060499547
geneview	rs1060499547
scholar	rs1060499547
google	rs1060499547
pharmgkb	rs1060499547
gwascentral	rs1060499547
openSNP	rs1060499547
23andMe	rs1060499547
SNPshot	rs1060499547
SNPdbe	rs1060499547
MSV3d	rs1060499547
GWAS Ctlg	rs1060499547

Max Magnitude

0

ClinVar
Risk	rs1060499547(G;G)
Alt	rs1060499547(G;G)
Reference	Rs1060499547(A;A)
Significance	Pathogenic
Disease	Abnormality of skeletal morphology Congenital heart disease Failure to thrive
Variation	info
Gene	ABL1
CLNDBN	Abnormality of skeletal morphology Congenital heart disease Failure to thrive
Reversed	0
HGVS	NC_000009.11:g.133738277A>G
CLNSRC
CLNACC	RCV000445576.1,