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

rs730880403

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880403(A;A)
Make rs730880403(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34791152
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880403
ebirs730880403
HLIrs730880403
Exacrs730880403
Varsomers730880403
Maprs730880403
PheGenIrs730880403
hapmaprs730880403
1000 genomesrs730880403
hgdprs730880403
ensemblrs730880403
gopubmedrs730880403
geneviewrs730880403
scholarrs730880403
googlers730880403
pharmgkbrs730880403
gwascentralrs730880403
openSNPrs730880403
23andMers730880403
23andMe allrs730880403
SNP Nexus

SNPshotrs730880403
SNPdbers730880403
MSV3drs730880403
GWAS Ctlgrs730880403
Max Magnitude0
ClinVar
Risk rs730880403(A;A)
Alt rs730880403(A;A)
Reference rs730880403(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.35083353C>T
CLNSRC
CLNACC RCV000157798.1,