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rs786201040

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201040(C;T)
Make rs786201040(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position86923600
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs786201040
dbSNP (classic)rs786201040
ClinGenrs786201040
ebirs786201040
HLIrs786201040
Exacrs786201040
Gnomadrs786201040
Varsomers786201040
LitVarrs786201040
Maprs786201040
PheGenIrs786201040
Biobankrs786201040
1000 genomesrs786201040
hgdprs786201040
ensemblrs786201040
geneviewrs786201040
scholarrs786201040
googlers786201040
pharmgkbrs786201040
gwascentralrs786201040
openSNPrs786201040
23andMers786201040
SNPshotrs786201040
SNPdbers786201040
MSV3drs786201040
GWAS Ctlgrs786201040
Max Magnitude0
ClinVar
Risk rs786201040(T;T)
Alt rs786201040(T;T)
Reference Rs786201040(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BMPR1A
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.88683357C>T
CLNSRC
CLNACC RCV000162419.2, RCV000483189.1,