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rs1057519418

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519418(A;C)
Make rs1057519418(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position8534399
GeneANOS1
is asnp
is mentioned by
dbSNPrs1057519418
dbSNP (old)rs1057519418
ClinGenrs1057519418
ebirs1057519418
HLIrs1057519418
Exacrs1057519418
Gnomadrs1057519418
Varsomers1057519418
Maprs1057519418
PheGenIrs1057519418
Biobankrs1057519418
1000 genomesrs1057519418
hgdprs1057519418
ensemblrs1057519418
gopubmedrs1057519418
geneviewrs1057519418
scholarrs1057519418
googlers1057519418
pharmgkbrs1057519418
gwascentralrs1057519418
openSNPrs1057519418
23andMers1057519418
23andMe allrs1057519418
SNPshotrs1057519418
SNPdbers1057519418
MSV3drs1057519418
GWAS Ctlgrs1057519418
Max Magnitude0
ClinVar
Risk rs1057519418(C;C)
Alt rs1057519418(C;C)
Reference Rs1057519418(A;A)
Significance Probable-Pathogenic
Disease Kallmann syndrome 1
Variation info
Gene ANOS1
CLNDBN Kallmann syndrome 1
Reversed 1
HGVS NC_000023.10:g.8502440T>G
CLNSRC
CLNACC RCV000416541.1,