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rs387906389

From SNPedia

Orientationplus
Geno Mag Summary
(GATGA;GATGA) 0 common in clinvar
Make rs387906389(-;-)
Make rs387906389(-;GATGA)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position51986840
GeneACVR1B
is asnp
is mentioned by
dbSNPrs387906389
ebirs387906389
HLIrs387906389
Exacrs387906389
Varsomers387906389
Maprs387906389
PheGenIrs387906389
hapmaprs387906389
1000 genomesrs387906389
hgdprs387906389
ensemblrs387906389
gopubmedrs387906389
geneviewrs387906389
scholarrs387906389
googlers387906389
pharmgkbrs387906389
gwascentralrs387906389
openSNPrs387906389
23andMers387906389
23andMe allrs387906389
SNP Nexus

SNPshotrs387906389
SNPdbers387906389
MSV3drs387906389
GWAS Ctlgrs387906389
Max Magnitude0
ClinVar
Risk rs387906389(;)
Alt rs387906389(;)
Reference rs387906389(GATGA;GATGA)
Significance Pathogenic
Disease Carcinoma of pancreas
Variation info
Gene ACVR1B
CLNDBN Carcinoma of pancreas
Reversed 0
HGVS NC_000012.11:g.52380624_52380628delGATGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008710.4,