Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880388

From SNPedia

Orientationminus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
Make rs730880388(-;-)
Make rs730880388(-;TCT)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34793422
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880388
ebirs730880388
HLIrs730880388
Exacrs730880388
Varsomers730880388
Maprs730880388
PheGenIrs730880388
hapmaprs730880388
1000 genomesrs730880388
hgdprs730880388
ensemblrs730880388
gopubmedrs730880388
geneviewrs730880388
scholarrs730880388
googlers730880388
pharmgkbrs730880388
gwascentralrs730880388
openSNPrs730880388
23andMers730880388
23andMe allrs730880388
SNP Nexus

SNPshotrs730880388
SNPdbers730880388
MSV3drs730880388
GWAS Ctlgrs730880388
Max Magnitude0
ClinVar
Risk rs730880388(;)
Alt rs730880388(;)
Reference rs730880388(TCT;TCT)
Significance Other
Disease not provided
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.35085623_35085625delAGA
CLNSRC
CLNACC RCV000157773.1,