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rs606231409

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231409(A;G)
Make rs606231409(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position8732036
GeneANOS1
is asnp
is mentioned by
dbSNPrs606231409
ebirs606231409
HLIrs606231409
Exacrs606231409
Varsomers606231409
Maprs606231409
PheGenIrs606231409
hapmaprs606231409
1000 genomesrs606231409
hgdprs606231409
ensemblrs606231409
gopubmedrs606231409
geneviewrs606231409
scholarrs606231409
googlers606231409
pharmgkbrs606231409
gwascentralrs606231409
openSNPrs606231409
23andMers606231409
23andMe allrs606231409
SNP Nexus

SNPshotrs606231409
SNPdbers606231409
MSV3drs606231409
GWAS Ctlgrs606231409
Max Magnitude0
ClinVar
Risk rs606231409(G;G)
Alt rs606231409(G;G)
Reference rs606231409(A;A)
Significance Pathogenic
Disease Kallmann syndrome 1
Variation info
Gene KAL1 ANOS1
CLNDBN Kallmann syndrome 1
Reversed 1
HGVS NC_000023.10:g.8700077T>C
CLNSRC VariO
CLNACC RCV000128830.1,