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rs1057520610

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520610(G;T)
Make rs1057520610(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position64192716
GeneAMER1
is asnp
is mentioned by
dbSNPrs1057520610
dbSNP (old)rs1057520610
ClinGenrs1057520610
ebirs1057520610
HLIrs1057520610
Exacrs1057520610
Gnomadrs1057520610
Varsomers1057520610
LitVarrs1057520610
Maprs1057520610
PheGenIrs1057520610
Biobankrs1057520610
1000 genomesrs1057520610
hgdprs1057520610
ensemblrs1057520610
gopubmedrs1057520610
geneviewrs1057520610
scholarrs1057520610
googlers1057520610
pharmgkbrs1057520610
gwascentralrs1057520610
openSNPrs1057520610
23andMers1057520610
23andMe allrs1057520610
SNPshotrs1057520610
SNPdbers1057520610
MSV3drs1057520610
GWAS Ctlgrs1057520610
Max Magnitude0
ClinVar
Risk rs1057520610(T;T)
Alt rs1057520610(T;T)
Reference Rs1057520610(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AMER1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.63412596C>A
CLNSRC
CLNACC RCV000443715.1,