Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852214
rs137852214
ZDHHC9
1.000 X 129823724 missense variant G/A snv
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.800 0
dbSNP: rs137852215
rs137852215
ZDHHC9
1.000 X 129823718 missense variant G/A snv
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.800 0
dbSNP: rs1131690786
rs1131690786
ZDHHC9
1.000 X 129829023 missense variant G/A snv
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.700 0
dbSNP: rs1569321518
rs1569321518
ZDHHC9
1.000 X 129829041 missense variant C/T snv
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.700 0
dbSNP: rs606231182
rs606231182
ZDHHC9
1.000 X 129829134 frameshift variant AGCG/- del
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.700 0
dbSNP: rs606231183
rs606231183
ZDHHC9
1.000 X 129841774 splice region variant C/G snv
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		0.700 0