Source: UNIPROT

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: rs864321627
rs864321627
TAF1
1.000 X 71401691 missense variant T/C snv
CUI: C4225418
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 33
MENTAL RETARDATION, X-LINKED, SYNDROMIC 33 		0.800 1.000 1 2015 2015
dbSNP: rs864321628
rs864321628
TAF1
1.000 X 71387393 missense variant T/C snv
CUI: C4225418
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 33
MENTAL RETARDATION, X-LINKED, SYNDROMIC 33 		0.800 1.000 1 2015 2015
dbSNP: rs864321629
rs864321629
TAF1
1.000 X 71398627 missense variant C/T snv
CUI: C4225418
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 33
MENTAL RETARDATION, X-LINKED, SYNDROMIC 33 		0.800 1.000 1 2015 2015
dbSNP: rs864321630
rs864321630
TAF1
1.000 X 71382821 missense variant C/T snv
CUI: C4225418
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 33
MENTAL RETARDATION, X-LINKED, SYNDROMIC 33 		0.800 1.000 1 2015 2015
dbSNP: rs864321631
rs864321631
TAF1
1.000 X 71392653 missense variant G/C snv
CUI: C4225418
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 33
MENTAL RETARDATION, X-LINKED, SYNDROMIC 33 		0.800 1.000 1 2015 2015