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rs1057520166

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520166(C;T)
Make rs1057520166(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position48995830
GeneARFGEF2
is asnp
is mentioned by
dbSNPrs1057520166
dbSNP (classic)rs1057520166
ClinGenrs1057520166
ebirs1057520166
HLIrs1057520166
Exacrs1057520166
Gnomadrs1057520166
Varsomers1057520166
LitVarrs1057520166
Maprs1057520166
PheGenIrs1057520166
Biobankrs1057520166
1000 genomesrs1057520166
hgdprs1057520166
ensemblrs1057520166
geneviewrs1057520166
scholarrs1057520166
googlers1057520166
pharmgkbrs1057520166
gwascentralrs1057520166
openSNPrs1057520166
23andMers1057520166
23andMe allrs1057520166
SNPshotrs1057520166
SNPdbers1057520166
MSV3drs1057520166
GWAS Ctlgrs1057520166
Max Magnitude0
ClinVar
Risk rs1057520166(T;T)
Alt rs1057520166(T;T)
Reference Rs1057520166(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARFGEF2
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.47612367C>T
CLNSRC
CLNACC RCV000438084.1,