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rs1057519875

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519875(G;T)
Make rs1057519875(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position157770385
GeneACVR1
is asnp
is mentioned by
dbSNPrs1057519875
dbSNP (classic)rs1057519875
ClinGenrs1057519875
ebirs1057519875
HLIrs1057519875
Exacrs1057519875
Gnomadrs1057519875
Varsomers1057519875
LitVarrs1057519875
Maprs1057519875
PheGenIrs1057519875
Biobankrs1057519875
1000 genomesrs1057519875
hgdprs1057519875
ensemblrs1057519875
geneviewrs1057519875
scholarrs1057519875
googlers1057519875
pharmgkbrs1057519875
gwascentralrs1057519875
openSNPrs1057519875
23andMers1057519875
SNPshotrs1057519875
SNPdbers1057519875
MSV3drs1057519875
GWAS Ctlgrs1057519875
Max Magnitude0
ClinVar
Risk rs1057519875(T;T)
Alt rs1057519875(T;T)
Reference Rs1057519875(G;G)
Significance Probable-Pathogenic
Disease Adenocarcinoma of stomach Brainstem glioma
Variation info
Gene ACVR1
CLNDBN Adenocarcinoma of stomach Brainstem glioma
Reversed 1
HGVS NC_000002.11:g.158626897C>A
CLNSRC
CLNACC RCV000426291.1, RCV000444963.1,