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rs730880962

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880962(A;A)
Make rs730880962(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46858425
GeneMYL3
is asnp
is mentioned by
dbSNPrs730880962
ebirs730880962
HLIrs730880962
Exacrs730880962
Varsomers730880962
Maprs730880962
PheGenIrs730880962
hapmaprs730880962
1000 genomesrs730880962
hgdprs730880962
ensemblrs730880962
gopubmedrs730880962
geneviewrs730880962
scholarrs730880962
googlers730880962
pharmgkbrs730880962
gwascentralrs730880962
openSNPrs730880962
23andMers730880962
23andMe allrs730880962
SNP Nexus

SNPshotrs730880962
SNPdbers730880962
MSV3drs730880962
GWAS Ctlgrs730880962
Max Magnitude0
ClinVar
Risk rs730880962(A;A)
Alt rs730880962(A;A)
Reference rs730880962(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYL3
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.46899915A>T
CLNSRC
CLNACC RCV000158962.1,