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rs1057520209

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520209(C;C)
Make rs1057520209(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position8731892
GeneANOS1
is asnp
is mentioned by
dbSNPrs1057520209
dbSNP (classic)rs1057520209
ClinGenrs1057520209
ebirs1057520209
HLIrs1057520209
Exacrs1057520209
Gnomadrs1057520209
Varsomers1057520209
LitVarrs1057520209
Maprs1057520209
PheGenIrs1057520209
Biobankrs1057520209
1000 genomesrs1057520209
hgdprs1057520209
ensemblrs1057520209
geneviewrs1057520209
scholarrs1057520209
googlers1057520209
pharmgkbrs1057520209
gwascentralrs1057520209
openSNPrs1057520209
23andMers1057520209
23andMe allrs1057520209
SNPshotrs1057520209
SNPdbers1057520209
MSV3drs1057520209
GWAS Ctlgrs1057520209
Max Magnitude0
ClinVar
Risk rs1057520209(C;C)
Alt rs1057520209(C;C)
Reference Rs1057520209(T;T)
Significance Probable-Pathogenic
Disease Kallmann syndrome 1
Variation info
Gene KAL1 ANOS1
CLNDBN Kallmann syndrome 1
Reversed 1
HGVS NC_000023.10:g.8699933A>G
CLNSRC
CLNACC RCV000445562.1,