Have questions? Visit https://www.reddit.com/r/SNPedia

rs397517063

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517063(A;A)
Make rs397517063(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34792549
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs397517063
ebirs397517063
HLIrs397517063
Exacrs397517063
Varsomers397517063
Maprs397517063
PheGenIrs397517063
hapmaprs397517063
1000 genomesrs397517063
hgdprs397517063
ensemblrs397517063
gopubmedrs397517063
geneviewrs397517063
scholarrs397517063
googlers397517063
pharmgkbrs397517063
gwascentralrs397517063
openSNPrs397517063
23andMers397517063
23andMe allrs397517063
SNP Nexus

SNPshotrs397517063
SNPdbers397517063
MSV3drs397517063
GWAS Ctlgrs397517063
Max Magnitude0
ClinVar
Risk rs397517063(A;A)
Alt rs397517063(A;A)
Reference rs397517063(G;G)
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.35084750C>T
CLNSRC
CLNACC RCV000038330.2, RCV000157781.1,