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rs730880955

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880955(C;G)
Make rs730880955(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46860789
GeneMYL3
is asnp
is mentioned by
dbSNPrs730880955
ebirs730880955
HLIrs730880955
Exacrs730880955
Varsomers730880955
Maprs730880955
PheGenIrs730880955
hapmaprs730880955
1000 genomesrs730880955
hgdprs730880955
ensemblrs730880955
gopubmedrs730880955
geneviewrs730880955
scholarrs730880955
googlers730880955
pharmgkbrs730880955
gwascentralrs730880955
openSNPrs730880955
23andMers730880955
23andMe allrs730880955
SNP Nexus

SNPshotrs730880955
SNPdbers730880955
MSV3drs730880955
GWAS Ctlgrs730880955
Max Magnitude0
ClinVar
Risk rs730880955(G;G)
Alt rs730880955(G;G)
Reference rs730880955(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYL3
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.46902279G>C
CLNSRC
CLNACC RCV000158941.2,