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rs1057524703

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524703(A;C)
Make rs1057524703(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position81511353
GeneACTG1, FSCN2
is asnp
is mentioned by
dbSNPrs1057524703
dbSNP (classic)rs1057524703
ClinGenrs1057524703
ebirs1057524703
HLIrs1057524703
Exacrs1057524703
Gnomadrs1057524703
Varsomers1057524703
LitVarrs1057524703
Maprs1057524703
PheGenIrs1057524703
Biobankrs1057524703
1000 genomesrs1057524703
hgdprs1057524703
ensemblrs1057524703
geneviewrs1057524703
scholarrs1057524703
googlers1057524703
pharmgkbrs1057524703
gwascentralrs1057524703
openSNPrs1057524703
23andMers1057524703
23andMe allrs1057524703
SNPshotrs1057524703
SNPdbers1057524703
MSV3drs1057524703
GWAS Ctlgrs1057524703
Max Magnitude0
ClinVar
Risk rs1057524703(C;C)
Alt rs1057524703(C;C)
Reference Rs1057524703(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTG1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.79478379T>G
CLNSRC
CLNACC RCV000444848.1,