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rs886041756

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome17
Position81511048
GeneACTG1, FSCN2
is asnp
is mentioned by
dbSNPrs886041756
dbSNP (classic)rs886041756
ClinGenrs886041756
ebirs886041756
HLIrs886041756
Exacrs886041756
Gnomadrs886041756
Varsomers886041756
LitVarrs886041756
Maprs886041756
PheGenIrs886041756
Biobankrs886041756
1000 genomesrs886041756
hgdprs886041756
ensemblrs886041756
geneviewrs886041756
scholarrs886041756
googlers886041756
pharmgkbrs886041756
gwascentralrs886041756
openSNPrs886041756
23andMers886041756
23andMe allrs886041756
SNPshotrs886041756
SNPdbers886041756
MSV3drs886041756
GWAS Ctlgrs886041756
Max Magnitude0
ClinVar
Risk rs886041756(G;G)
Alt rs886041756(G;G)
Reference Rs886041756(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTG1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.79478074T>C
CLNSRC
CLNACC RCV000293975.1,