rs367543035

Orientation

plus

Stabilized

plus

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

Make rs367543035(-;-)

Make rs367543035(-;CAA)

Reference

GRCh38 38.1/141

Chromosome

15

Position

90749825

Gene

BLM

is a	snp
is	mentioned by
dbSNP	rs367543035
dbSNP (classic)	rs367543035
ClinGen	rs367543035
ebi	rs367543035
HLI	rs367543035
Exac	rs367543035
Gnomad	rs367543035
Varsome	rs367543035
LitVar	rs367543035
Map	rs367543035
PheGenI	rs367543035
Biobank	rs367543035
1000 genomes	rs367543035
hgdp	rs367543035
ensembl	rs367543035
geneview	rs367543035
scholar	rs367543035
google	rs367543035
pharmgkb	rs367543035
gwascentral	rs367543035
openSNP	rs367543035
23andMe	rs367543035
SNPshot	rs367543035
SNPdbe	rs367543035
MSV3d	rs367543035
GWAS Ctlg	rs367543035

Max Magnitude

0

ClinVar
Risk	rs367543035(-;-)
Alt	rs367543035(-;-)
Reference	Rs367543035(CAA;CAA)
Significance	Pathogenic
Disease	Bloom syndrome
Variation	info
Gene	BLM
CLNDBN	Bloom syndrome
Reversed	0
HGVS	NC_000015.9:g.91293055_91293057delCAA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005788.2,