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: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C4025190
Disease: Abnormal epiglottis morphology
Abnormal epiglottis morphology
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
Abnormality of nasopharyngeal adenoids
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C4024158
Disease: Abnormality of the columella
Abnormality of the columella
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
Abnormality of the tympanic membrane
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0003467
Disease: Anxiety
Anxiety
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C3809650
Disease: BAINBRIDGE-ROPERS SYNDROME
BAINBRIDGE-ROPERS SYNDROME
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C1867131
Disease: Broad hallux
Broad hallux
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0426891
Disease: Broad thumbs
Broad thumbs
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0856863
Disease: Broad-based gait
Broad-based gait
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C1845447
Disease: Cupped ears (finding)
Cupped ears (finding)
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C4023801
Disease: Fibular bowing
Fibular bowing
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0016202
Disease: Flatfoot
Flatfoot
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0333068
Disease: Flexion contracture
Flexion contracture
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
Flexion contracture of proximal interphalangeal joint
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0267048
Disease: Glossoptosis
Glossoptosis
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C0456070
Disease: Growth delay
Growth delay
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow
0.700 1.000 1 2016 2016
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C1846176
Disease: Hyperactive deep tendon reflexes
Hyperactive deep tendon reflexes
0.700 1.000 1 2016 2016