rs1057517374

Orientation

plus

Stabilized

plus

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

Make rs1057517374(-;-)

Make rs1057517374(-;CA)

Make rs1057517374(CA;CA)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

90749566

Gene

BLM

is a	snp
is	mentioned by
dbSNP	rs1057517374
dbSNP (classic)	rs1057517374
ClinGen	rs1057517374
ebi	rs1057517374
HLI	rs1057517374
Exac	rs1057517374
Gnomad	rs1057517374
Varsome	rs1057517374
LitVar	rs1057517374
Map	rs1057517374
PheGenI	rs1057517374
Biobank	rs1057517374
1000 genomes	rs1057517374
hgdp	rs1057517374
ensembl	rs1057517374
geneview	rs1057517374
scholar	rs1057517374
google	rs1057517374
pharmgkb	rs1057517374
gwascentral	rs1057517374
openSNP	rs1057517374
23andMe	rs1057517374
SNPshot	rs1057517374
SNPdbe	rs1057517374
MSV3d	rs1057517374
GWAS Ctlg	rs1057517374

Max Magnitude

0

ClinVar
Risk	rs1057517374(-;-)
Alt	rs1057517374(-;-)
Reference	Rs1057517374(AC;AC)
Significance	Probable-Pathogenic
Disease	Bloom syndrome
Variation	info
Gene	BLM
CLNDBN	Bloom syndrome
Reversed	0
HGVS	NC_000015.9:g.91292796_91292797delCA
CLNSRC
CLNACC	RCV000411055.1,