Gene: HHAT ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7527939
rs7527939
HHAT
1 1.000 0.040 1 210362681 intron variant C/T snv 0.30 0.810 1.000 1 2013 2013