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rs398123562

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123562(G;T)
Make rs398123562(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position229432877
GeneACTA1
is asnp
is mentioned by
dbSNPrs398123562
ebirs398123562
HLIrs398123562
Exacrs398123562
Varsomers398123562
Maprs398123562
PheGenIrs398123562
hapmaprs398123562
1000 genomesrs398123562
hgdprs398123562
ensemblrs398123562
gopubmedrs398123562
geneviewrs398123562
scholarrs398123562
googlers398123562
pharmgkbrs398123562
gwascentralrs398123562
openSNPrs398123562
23andMers398123562
23andMe allrs398123562
SNP Nexus

SNPshotrs398123562
SNPdbers398123562
MSV3drs398123562
GWAS Ctlgrs398123562
Max Magnitude0
ClinVar
Risk rs398123562(T;T)
Alt rs398123562(T;T)
Reference rs398123562(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.229568624C>A
CLNSRC HGMD
CLNACC RCV000079464.4,