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rs786204471

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204471(-;-)
Make rs786204471(-;AAAT)
Make rs786204471(AAAT;AAAT)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position90766966
GeneBLM
is asnp
is mentioned by
dbSNPrs786204471
ebirs786204471
HLIrs786204471
Exacrs786204471
Varsomers786204471
Maprs786204471
PheGenIrs786204471
hapmaprs786204471
1000 genomesrs786204471
hgdprs786204471
ensemblrs786204471
gopubmedrs786204471
geneviewrs786204471
scholarrs786204471
googlers786204471
pharmgkbrs786204471
gwascentralrs786204471
openSNPrs786204471
23andMers786204471
23andMe allrs786204471
SNP Nexus

SNPshotrs786204471
SNPdbers786204471
MSV3drs786204471
GWAS Ctlgrs786204471
Max Magnitude0
ClinVar
Risk rs786204471(AAAT;AAAT)
Alt rs786204471(AAAT;AAAT)
Reference rs786204471(;)
Significance Other
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91310196_91310197insAAAT
CLNSRC Counsyl
CLNACC RCV000169119.2,