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rs730880404

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880404(C;T)
Make rs730880404(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34791136
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880404
ebirs730880404
HLIrs730880404
Exacrs730880404
Varsomers730880404
Maprs730880404
PheGenIrs730880404
hapmaprs730880404
1000 genomesrs730880404
hgdprs730880404
ensemblrs730880404
gopubmedrs730880404
geneviewrs730880404
scholarrs730880404
googlers730880404
pharmgkbrs730880404
gwascentralrs730880404
openSNPrs730880404
23andMers730880404
23andMe allrs730880404
SNP Nexus

SNPshotrs730880404
SNPdbers730880404
MSV3drs730880404
GWAS Ctlgrs730880404
Max Magnitude0
ClinVar
Risk rs730880404(T;T)
Alt rs730880404(T;T)
Reference rs730880404(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.35083337G>A
CLNSRC
CLNACC RCV000157799.1,