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rs730880954

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880954(A;A)
Make rs730880954(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46860799
GeneMYL3
is asnp
is mentioned by
dbSNPrs730880954
ebirs730880954
HLIrs730880954
Exacrs730880954
Varsomers730880954
Maprs730880954
PheGenIrs730880954
hapmaprs730880954
1000 genomesrs730880954
hgdprs730880954
ensemblrs730880954
gopubmedrs730880954
geneviewrs730880954
scholarrs730880954
googlers730880954
pharmgkbrs730880954
gwascentralrs730880954
openSNPrs730880954
23andMers730880954
23andMe allrs730880954
SNP Nexus

SNPshotrs730880954
SNPdbers730880954
MSV3drs730880954
GWAS Ctlgrs730880954
Max Magnitude0
ClinVar
Risk rs730880954(A;A)
Alt rs730880954(A;A)
Reference rs730880954(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYL3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000003.11:g.46902289C>T
CLNSRC
CLNACC RCV000158939.2, RCV000214205.1,