rs1057517431

Orientation

plus

Stabilized

plus

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

Make rs1057517431(-;-)

Make rs1057517431(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

90761168

Gene

BLM

is a	snp
is	mentioned by
dbSNP	rs1057517431
dbSNP (classic)	rs1057517431
ClinGen	rs1057517431
ebi	rs1057517431
HLI	rs1057517431
Exac	rs1057517431
Gnomad	rs1057517431
Varsome	rs1057517431
LitVar	rs1057517431
Map	rs1057517431
PheGenI	rs1057517431
Biobank	rs1057517431
1000 genomes	rs1057517431
hgdp	rs1057517431
ensembl	rs1057517431
geneview	rs1057517431
scholar	rs1057517431
google	rs1057517431
pharmgkb	rs1057517431
gwascentral	rs1057517431
openSNP	rs1057517431
23andMe	rs1057517431
SNPshot	rs1057517431
SNPdbe	rs1057517431
MSV3d	rs1057517431
GWAS Ctlg	rs1057517431

Max Magnitude

0

ClinVar
Risk	rs1057517431(-;-)
Alt	rs1057517431(-;-)
Reference	Rs1057517431(A;A)
Significance	Probable-Pathogenic
Disease	Bloom syndrome
Variation	info
Gene	BLM
CLNDBN	Bloom syndrome
Reversed	0
HGVS	NC_000015.9:g.91304398delA
CLNSRC
CLNACC	RCV000411246.1,