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rs150421256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs150421256(A;G)
Make rs150421256(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position90811203
GeneBLM
is asnp
is mentioned by
dbSNPrs150421256
dbSNP (classic)rs150421256
ClinGenrs150421256
ebirs150421256
HLIrs150421256
Exacrs150421256
Gnomadrs150421256
Varsomers150421256
LitVarrs150421256
Maprs150421256
PheGenIrs150421256
Biobankrs150421256
1000 genomesrs150421256
hgdprs150421256
ensemblrs150421256
geneviewrs150421256
scholarrs150421256
googlers150421256
pharmgkbrs150421256
gwascentralrs150421256
openSNPrs150421256
23andMers150421256
23andMe allrs150421256
SNPshotrs150421256
SNPdbers150421256
MSV3drs150421256
GWAS Ctlgrs150421256
Max Magnitude0
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,