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rs886041280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position81512135
GeneACTG1, FSCN2
is asnp
is mentioned by
dbSNPrs886041280
dbSNP (classic)rs886041280
ClinGenrs886041280
ebirs886041280
HLIrs886041280
Exacrs886041280
Gnomadrs886041280
Varsomers886041280
LitVarrs886041280
Maprs886041280
PheGenIrs886041280
Biobankrs886041280
1000 genomesrs886041280
hgdprs886041280
ensemblrs886041280
geneviewrs886041280
scholarrs886041280
googlers886041280
pharmgkbrs886041280
gwascentralrs886041280
openSNPrs886041280
23andMers886041280
23andMe allrs886041280
SNPshotrs886041280
SNPdbers886041280
MSV3drs886041280
GWAS Ctlgrs886041280
Max Magnitude0
ClinVar
Risk rs886041280(A;A)
Alt rs886041280(A;A)
Reference Rs886041280(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FSCN2 ACTG1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.79479161A>T
CLNSRC
CLNACC RCV000390797.1,