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rs397517059

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517059(C;T)
Make rs397517059(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position34793389
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs397517059
dbSNP (classic)rs397517059
ClinGenrs397517059
ebirs397517059
HLIrs397517059
Exacrs397517059
Gnomadrs397517059
Varsomers397517059
LitVarrs397517059
Maprs397517059
PheGenIrs397517059
Biobankrs397517059
1000 genomesrs397517059
hgdprs397517059
ensemblrs397517059
geneviewrs397517059
scholarrs397517059
googlers397517059
pharmgkbrs397517059
gwascentralrs397517059
openSNPrs397517059
23andMers397517059
SNPshotrs397517059
SNPdbers397517059
MSV3drs397517059
GWAS Ctlgrs397517059
Max Magnitude0
ClinVar
Risk rs397517059(T;T)
Alt rs397517059(T;T)
Reference Rs397517059(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not specified not provided
Reversed 1
HGVS NC_000015.9:g.35085590G>A
CLNSRC
CLNACC RCV000038325.3, RCV000484679.1,