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rs1057520694

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520694(C;T)
Make rs1057520694(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position73913617
GeneACTG2
is asnp
is mentioned by
dbSNPrs1057520694
dbSNP (old)rs1057520694
ClinGenrs1057520694
ebirs1057520694
HLIrs1057520694
Exacrs1057520694
Gnomadrs1057520694
Varsomers1057520694
Maprs1057520694
PheGenIrs1057520694
Biobankrs1057520694
1000 genomesrs1057520694
hgdprs1057520694
ensemblrs1057520694
gopubmedrs1057520694
geneviewrs1057520694
scholarrs1057520694
googlers1057520694
pharmgkbrs1057520694
gwascentralrs1057520694
openSNPrs1057520694
23andMers1057520694
23andMe allrs1057520694
SNPshotrs1057520694
SNPdbers1057520694
MSV3drs1057520694
GWAS Ctlgrs1057520694
Max Magnitude0
ClinVar
Risk rs1057520694(T;T)
Alt rs1057520694(T;T)
Reference Rs1057520694(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACTG2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.74140744C>T
CLNSRC
CLNACC RCV000430933.1,