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rs786204640

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs786204640(-;-)
Make rs786204640(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position90749849
GeneBLM
is asnp
is mentioned by
dbSNPrs786204640
ebirs786204640
HLIrs786204640
Exacrs786204640
Varsomers786204640
Maprs786204640
PheGenIrs786204640
hapmaprs786204640
1000 genomesrs786204640
hgdprs786204640
ensemblrs786204640
gopubmedrs786204640
geneviewrs786204640
scholarrs786204640
googlers786204640
pharmgkbrs786204640
gwascentralrs786204640
openSNPrs786204640
23andMers786204640
23andMe allrs786204640
SNP Nexus

SNPshotrs786204640
SNPdbers786204640
MSV3drs786204640
GWAS Ctlgrs786204640
Max Magnitude0
ClinVar
Risk rs786204640(;)
Alt rs786204640(;)
Reference rs786204640(TT;TT)
Significance Probable-Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91293079_91293080delTT
CLNSRC Counsyl
CLNACC RCV000169422.1,