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rs606231179

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231179(-;-)
Make rs606231179(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeY
Position2787280
GeneSRY
is asnp
is mentioned by
dbSNPrs606231179
ebirs606231179
HLIrs606231179
Exacrs606231179
Varsomers606231179
Maprs606231179
PheGenIrs606231179
hapmaprs606231179
1000 genomesrs606231179
hgdprs606231179
ensemblrs606231179
gopubmedrs606231179
geneviewrs606231179
scholarrs606231179
googlers606231179
pharmgkbrs606231179
gwascentralrs606231179
openSNPrs606231179
23andMers606231179
23andMe allrs606231179
SNP Nexus

SNPshotrs606231179
SNPdbers606231179
MSV3drs606231179
GWAS Ctlgrs606231179
Y Chromrs606231179
Max Magnitude0
ClinVar
Risk rs606231179(;)
Alt rs606231179(;)
Reference rs606231179(A;A)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655321delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000010397.5,