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rs1057519602

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057519602(-;-)
Make rs1057519602(-;GA)
Make rs1057519602(GA;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position200571799
GeneSGO2
is asnp
is mentioned by
dbSNPrs1057519602
dbSNP (old)rs1057519602
ClinGenrs1057519602
ebirs1057519602
HLIrs1057519602
Exacrs1057519602
Gnomadrs1057519602
Varsomers1057519602
Maprs1057519602
PheGenIrs1057519602
Biobankrs1057519602
1000 genomesrs1057519602
hgdprs1057519602
ensemblrs1057519602
gopubmedrs1057519602
geneviewrs1057519602
scholarrs1057519602
googlers1057519602
pharmgkbrs1057519602
gwascentralrs1057519602
openSNPrs1057519602
23andMers1057519602
23andMe allrs1057519602
SNPshotrs1057519602
SNPdbers1057519602
MSV3drs1057519602
GWAS Ctlgrs1057519602
Max Magnitude0
ClinVar
Risk rs1057519602(-;-)
Alt rs1057519602(-;-)
Reference Rs1057519602(AG;AG)
Significance Pathogenic
Disease Perrault Syndrome Premature ovarian failure
Variation info
Gene SGOL2 SGO2
CLNDBN Perrault Syndrome Premature ovarian failure
Reversed 0
HGVS NC_000002.11:g.201436522_201436523delGA
CLNSRC
CLNACC RCV000417144.1, RCV000417157.1,