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rs730880392

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880392(A;G)
Make rs730880392(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34792495
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880392
ebirs730880392
HLIrs730880392
Exacrs730880392
Varsomers730880392
Maprs730880392
PheGenIrs730880392
hapmaprs730880392
1000 genomesrs730880392
hgdprs730880392
ensemblrs730880392
gopubmedrs730880392
geneviewrs730880392
scholarrs730880392
googlers730880392
pharmgkbrs730880392
gwascentralrs730880392
openSNPrs730880392
23andMers730880392
23andMe allrs730880392
SNP Nexus

SNPshotrs730880392
SNPdbers730880392
MSV3drs730880392
GWAS Ctlgrs730880392
Max Magnitude0
ClinVar
Risk rs730880392(G;G)
Alt rs730880392(G;G)
Reference rs730880392(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided not specified
Reversed 1
HGVS NC_000015.9:g.35084696T>C
CLNSRC
CLNACC RCV000157782.2, RCV000223764.1,