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rs758683062

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758683062(C;T)
Make rs758683062(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51913675
GeneACVRL1
is asnp
is mentioned by
dbSNPrs758683062
ebirs758683062
HLIrs758683062
Exacrs758683062
Varsomers758683062
Maprs758683062
PheGenIrs758683062
hapmaprs758683062
1000 genomesrs758683062
hgdprs758683062
ensemblrs758683062
gopubmedrs758683062
geneviewrs758683062
scholarrs758683062
googlers758683062
pharmgkbrs758683062
gwascentralrs758683062
openSNPrs758683062
23andMers758683062
23andMe allrs758683062
SNP Nexus

SNPshotrs758683062
SNPdbers758683062
MSV3drs758683062
GWAS Ctlgrs758683062
Max Magnitude0
ClinVar
Risk rs758683062(T;T)
Alt rs758683062(T;T)
Reference rs758683062(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACVRL1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52307459C>T
CLNSRC
CLNACC RCV000197164.1,