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rs730880410

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880410(C;C)
Make rs730880410(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position34791118
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880410
ebirs730880410
HLIrs730880410
Exacrs730880410
Varsomers730880410
Maprs730880410
PheGenIrs730880410
hapmaprs730880410
1000 genomesrs730880410
hgdprs730880410
ensemblrs730880410
gopubmedrs730880410
geneviewrs730880410
scholarrs730880410
googlers730880410
pharmgkbrs730880410
gwascentralrs730880410
openSNPrs730880410
23andMers730880410
23andMe allrs730880410
SNP Nexus

SNPshotrs730880410
SNPdbers730880410
MSV3drs730880410
GWAS Ctlgrs730880410
Max Magnitude0
ClinVar
Risk rs730880410(C;C)
Alt rs730880410(C;C)
Reference rs730880410(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.35083319A>G
CLNSRC
CLNACC RCV000157808.2,