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rs1057522054

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057522054(A;G)
Make rs1057522054(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position73908764
GeneACTG2
is asnp
is mentioned by
dbSNPrs1057522054
dbSNP (old)rs1057522054
ClinGenrs1057522054
ebirs1057522054
HLIrs1057522054
Exacrs1057522054
Gnomadrs1057522054
Varsomers1057522054
Maprs1057522054
PheGenIrs1057522054
Biobankrs1057522054
1000 genomesrs1057522054
hgdprs1057522054
ensemblrs1057522054
gopubmedrs1057522054
geneviewrs1057522054
scholarrs1057522054
googlers1057522054
pharmgkbrs1057522054
gwascentralrs1057522054
openSNPrs1057522054
23andMers1057522054
23andMe allrs1057522054
SNPshotrs1057522054
SNPdbers1057522054
MSV3drs1057522054
GWAS Ctlgrs1057522054
Max Magnitude0
ClinVar
Risk rs1057522054(G;G)
Alt rs1057522054(G;G)
Reference Rs1057522054(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTG2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.74135891A>G
CLNSRC
CLNACC RCV000437539.1,