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rs730880407

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880407(C;C)
Make rs730880407(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34790434
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880407
ebirs730880407
HLIrs730880407
Exacrs730880407
Varsomers730880407
Maprs730880407
PheGenIrs730880407
hapmaprs730880407
1000 genomesrs730880407
hgdprs730880407
ensemblrs730880407
gopubmedrs730880407
geneviewrs730880407
scholarrs730880407
googlers730880407
pharmgkbrs730880407
gwascentralrs730880407
openSNPrs730880407
23andMers730880407
23andMe allrs730880407
SNP Nexus

SNPshotrs730880407
SNPdbers730880407
MSV3drs730880407
GWAS Ctlgrs730880407
Max Magnitude0
ClinVar
Risk rs730880407(C;C)
Alt rs730880407(C;C)
Reference rs730880407(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.35082635A>G
CLNSRC
CLNACC RCV000157802.1,