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rs764466442

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764466442(C;T)
Make rs764466442(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position86919384
GeneBMPR1A
is asnp
is mentioned by
dbSNPrs764466442
ebirs764466442
HLIrs764466442
Exacrs764466442
Varsomers764466442
Maprs764466442
PheGenIrs764466442
hapmaprs764466442
1000 genomesrs764466442
hgdprs764466442
ensemblrs764466442
gopubmedrs764466442
geneviewrs764466442
scholarrs764466442
googlers764466442
pharmgkbrs764466442
gwascentralrs764466442
openSNPrs764466442
23andMers764466442
23andMe allrs764466442
SNP Nexus

SNPshotrs764466442
SNPdbers764466442
MSV3drs764466442
GWAS Ctlgrs764466442
Max Magnitude0
ClinVar
Risk rs764466442(T;T)
Alt rs764466442(T;T)
Reference rs764466442(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BMPR1A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.88679141C>T
CLNSRC
CLNACC RCV000162430.1,