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rs730880401

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880401(C;C)
Make rs730880401(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34791292
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880401
ebirs730880401
HLIrs730880401
Exacrs730880401
Varsomers730880401
Maprs730880401
PheGenIrs730880401
hapmaprs730880401
1000 genomesrs730880401
hgdprs730880401
ensemblrs730880401
gopubmedrs730880401
geneviewrs730880401
scholarrs730880401
googlers730880401
pharmgkbrs730880401
gwascentralrs730880401
openSNPrs730880401
23andMers730880401
23andMe allrs730880401
SNP Nexus

SNPshotrs730880401
SNPdbers730880401
MSV3drs730880401
GWAS Ctlgrs730880401
Max Magnitude0
ClinVar
Risk rs730880401(C;C)
Alt rs730880401(C;C)
Reference rs730880401(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.35083493A>G
CLNSRC
CLNACC RCV000157795.1,