rs2197706, None

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Fragile X Syndrome
CUI: C0016667
Disease: Fragile X Syndrome
11 0.925 0.080 X 147813602 upstream gene variant A/C;T snv 0.700 1.000 1 2019 2019
FRAXA Syndrome
CUI: C0751156
Disease: FRAXA Syndrome
1 0.925 0.080 X 147813602 upstream gene variant A/C;T snv 0.700 1.000 1 2019 2019