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rs730880398

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880398(C;C)
Make rs730880398(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34792143
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880398
ebirs730880398
HLIrs730880398
Exacrs730880398
Varsomers730880398
Maprs730880398
PheGenIrs730880398
hapmaprs730880398
1000 genomesrs730880398
hgdprs730880398
ensemblrs730880398
gopubmedrs730880398
geneviewrs730880398
scholarrs730880398
googlers730880398
pharmgkbrs730880398
gwascentralrs730880398
openSNPrs730880398
23andMers730880398
23andMe allrs730880398
SNP Nexus

SNPshotrs730880398
SNPdbers730880398
MSV3drs730880398
GWAS Ctlgrs730880398
Max Magnitude0
ClinVar
Risk rs730880398(C;C)
Alt rs730880398(C;C)
Reference rs730880398(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.35084344A>G
CLNSRC
CLNACC RCV000157788.1,