rs367543014

Orientation

plus

Stabilized

plus

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

Make rs367543014(-;-)

Make rs367543014(-;C)

Reference

GRCh38 38.1/141

Chromosome

15

Position

90790748

Gene

BLM

is a	snp
is	mentioned by
dbSNP	rs367543014
dbSNP (classic)	rs367543014
ClinGen	rs367543014
ebi	rs367543014
HLI	rs367543014
Exac	rs367543014
Gnomad	rs367543014
Varsome	rs367543014
LitVar	rs367543014
Map	rs367543014
PheGenI	rs367543014
Biobank	rs367543014
1000 genomes	rs367543014
hgdp	rs367543014
ensembl	rs367543014
geneview	rs367543014
scholar	rs367543014
google	rs367543014
pharmgkb	rs367543014
gwascentral	rs367543014
openSNP	rs367543014
23andMe	rs367543014
SNPshot	rs367543014
SNPdbe	rs367543014
MSV3d	rs367543014
GWAS Ctlg	rs367543014

Max Magnitude

0

ClinVar
Risk	rs367543014(-;-)
Alt	rs367543014(-;-)
Reference	Rs367543014(C;C)
Significance	Pathogenic
Disease	Bloom syndrome not provided
Variation	info
Gene	BLM
CLNDBN	Bloom syndrome not provided
Reversed	0
HGVS	NC_000015.9:g.91333978delC
CLNSRC	ClinVar GeneDx GeneReviews
CLNACC	RCV000034902.2, RCV000115301.3,