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rs730880960

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880960(C;T)
Make rs730880960(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46860790
GeneMYL3
is asnp
is mentioned by
dbSNPrs730880960
ebirs730880960
HLIrs730880960
Exacrs730880960
Varsomers730880960
Maprs730880960
PheGenIrs730880960
hapmaprs730880960
1000 genomesrs730880960
hgdprs730880960
ensemblrs730880960
gopubmedrs730880960
geneviewrs730880960
scholarrs730880960
googlers730880960
pharmgkbrs730880960
gwascentralrs730880960
openSNPrs730880960
23andMers730880960
23andMe allrs730880960
SNP Nexus

SNPshotrs730880960
SNPdbers730880960
MSV3drs730880960
GWAS Ctlgrs730880960
Max Magnitude0
ClinVar
Risk rs730880960(T;T)
Alt rs730880960(T;T)
Reference rs730880960(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYL3
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.46902280G>A
CLNSRC
CLNACC RCV000158960.1,