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rs567723663

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs567723663(C;C)
Make rs567723663(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position46858471
GeneMYL3
is asnp
is mentioned by
dbSNPrs567723663
ebirs567723663
HLIrs567723663
Exacrs567723663
Varsomers567723663
Maprs567723663
PheGenIrs567723663
hapmaprs567723663
1000 genomesrs567723663
hgdprs567723663
ensemblrs567723663
gopubmedrs567723663
geneviewrs567723663
scholarrs567723663
googlers567723663
pharmgkbrs567723663
gwascentralrs567723663
openSNPrs567723663
23andMers567723663
23andMe allrs567723663
SNP Nexus

SNPshotrs567723663
SNPdbers567723663
MSV3drs567723663
GWAS Ctlgrs567723663
Max Magnitude0
ClinVar
Risk rs567723663(C;C)
Alt rs567723663(C;C)
Reference rs567723663(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYL3
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.46899961G>A
CLNSRC
CLNACC RCV000171360.1,