rs1057516774

Orientation

plus

Stabilized

plus

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

Make rs1057516774(G;T)

Make rs1057516774(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

90803562

Gene

BLM

is a	snp
is	mentioned by
dbSNP	rs1057516774
dbSNP (classic)	rs1057516774
ClinGen	rs1057516774
ebi	rs1057516774
HLI	rs1057516774
Exac	rs1057516774
Gnomad	rs1057516774
Varsome	rs1057516774
LitVar	rs1057516774
Map	rs1057516774
PheGenI	rs1057516774
Biobank	rs1057516774
1000 genomes	rs1057516774
hgdp	rs1057516774
ensembl	rs1057516774
geneview	rs1057516774
scholar	rs1057516774
google	rs1057516774
pharmgkb	rs1057516774
gwascentral	rs1057516774
openSNP	rs1057516774
23andMe	rs1057516774
SNPshot	rs1057516774
SNPdbe	rs1057516774
MSV3d	rs1057516774
GWAS Ctlg	rs1057516774

Max Magnitude

0

ClinVar
Risk	rs1057516774(T;T)
Alt	rs1057516774(T;T)
Reference	Rs1057516774(G;G)
Significance	Probable-Pathogenic
Disease	Bloom syndrome
Variation	info
Gene	BLM
CLNDBN	Bloom syndrome
Reversed	0
HGVS	NC_000015.9:g.91346792G>T
CLNSRC
CLNACC	RCV000412132.1,