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rs727503797

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503797(G;T)
Make rs727503797(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position229432350
GeneACTA1
is asnp
is mentioned by
dbSNPrs727503797
ebirs727503797
HLIrs727503797
Exacrs727503797
Varsomers727503797
Maprs727503797
PheGenIrs727503797
hapmaprs727503797
1000 genomesrs727503797
hgdprs727503797
ensemblrs727503797
gopubmedrs727503797
geneviewrs727503797
scholarrs727503797
googlers727503797
pharmgkbrs727503797
gwascentralrs727503797
openSNPrs727503797
23andMers727503797
23andMe allrs727503797
SNP Nexus

SNPshotrs727503797
SNPdbers727503797
MSV3drs727503797
GWAS Ctlgrs727503797
Max Magnitude0
ClinVar
Risk rs727503797(T;T)
Alt rs727503797(T;T)
Reference rs727503797(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTA1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.229568097C>A
CLNSRC
CLNACC RCV000152746.3,