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rs730880408

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880408(C;C)
Make rs730880408(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34794799
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880408
ebirs730880408
HLIrs730880408
Exacrs730880408
Varsomers730880408
Maprs730880408
PheGenIrs730880408
hapmaprs730880408
1000 genomesrs730880408
hgdprs730880408
ensemblrs730880408
gopubmedrs730880408
geneviewrs730880408
scholarrs730880408
googlers730880408
pharmgkbrs730880408
gwascentralrs730880408
openSNPrs730880408
23andMers730880408
23andMe allrs730880408
SNP Nexus

SNPshotrs730880408
SNPdbers730880408
MSV3drs730880408
GWAS Ctlgrs730880408
Max Magnitude0
ClinVar
Risk rs730880408(C;C)
Alt rs730880408(C;C)
Reference rs730880408(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.35087000C>G
CLNSRC
CLNACC RCV000157803.1,