rs150421256

Orientation

plus

Stabilized

plus

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

Make rs150421256(A;G)

Make rs150421256(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

90811203

Gene

BLM

is a	snp
is	mentioned by
dbSNP	rs150421256
dbSNP (classic)	rs150421256
ClinGen	rs150421256
ebi	rs150421256
HLI	rs150421256
Exac	rs150421256
Gnomad	rs150421256
Varsome	rs150421256
LitVar	rs150421256
Map	rs150421256
PheGenI	rs150421256
Biobank	rs150421256
1000 genomes	rs150421256
hgdp	rs150421256
ensembl	rs150421256
geneview	rs150421256
scholar	rs150421256
google	rs150421256
pharmgkb	rs150421256
gwascentral	rs150421256
openSNP	rs150421256
23andMe	rs150421256
SNPshot	rs150421256
SNPdbe	rs150421256
MSV3d	rs150421256
GWAS Ctlg	rs150421256

Max Magnitude

0

ClinVar
Risk	rs150421256(G;G)
Alt	rs150421256(G;G)
Reference	Rs150421256(A;A)
Significance	Probable-Pathogenic
Disease	Bloom syndrome
Variation	info
Gene	BLM
CLNDBN	Bloom syndrome
Reversed	0
HGVS	NC_000015.9:g.91354433A>G
CLNSRC
CLNACC	RCV000409613.1,