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rs1057518086

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518086(C;C)
Make rs1057518086(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position81512312
GeneACTG1, FSCN2
is asnp
is mentioned by
dbSNPrs1057518086
dbSNP (old)rs1057518086
ClinGenrs1057518086
ebirs1057518086
HLIrs1057518086
Exacrs1057518086
Gnomadrs1057518086
Varsomers1057518086
LitVarrs1057518086
Maprs1057518086
PheGenIrs1057518086
Biobankrs1057518086
1000 genomesrs1057518086
hgdprs1057518086
ensemblrs1057518086
gopubmedrs1057518086
geneviewrs1057518086
scholarrs1057518086
googlers1057518086
pharmgkbrs1057518086
gwascentralrs1057518086
openSNPrs1057518086
23andMers1057518086
23andMe allrs1057518086
SNPshotrs1057518086
SNPdbers1057518086
MSV3drs1057518086
GWAS Ctlgrs1057518086
Max Magnitude0
ClinVar
Risk rs1057518086(C;C)
Alt rs1057518086(C;C)
Reference Rs1057518086(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FSCN2 ACTG1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.79479338C>G
CLNSRC
CLNACC RCV000413555.1,