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rs730880406

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880406(C;T)
Make rs730880406(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34790548
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880406
ebirs730880406
HLIrs730880406
Exacrs730880406
Varsomers730880406
Maprs730880406
PheGenIrs730880406
hapmaprs730880406
1000 genomesrs730880406
hgdprs730880406
ensemblrs730880406
gopubmedrs730880406
geneviewrs730880406
scholarrs730880406
googlers730880406
pharmgkbrs730880406
gwascentralrs730880406
openSNPrs730880406
23andMers730880406
23andMe allrs730880406
SNP Nexus

SNPshotrs730880406
SNPdbers730880406
MSV3drs730880406
GWAS Ctlgrs730880406
Max Magnitude0
ClinVar
Risk rs730880406(T;T)
Alt rs730880406(T;T)
Reference rs730880406(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.35082749G>A
CLNSRC
CLNACC RCV000157801.1,