rs3135718, FGFR2

N. diseases: 4
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.882 0.160 10 121594355 intron variant C/T snv 0.54 0.700 1.000 1 2016 2016
Estrogen Receptor Status - Clinical Trial Eligibility Criteria
CUI: C1516974
Disease: Estrogen Receptor Status - Clinical Trial Eligibility Criteria
2 0.882 0.160 10 121594355 intron variant C/T snv 0.54 0.700 1.000 1 2016 2016
Congenital Microtia
CUI: C3850155
Disease: Congenital Microtia
1 0.882 0.160 10 121594355 intron variant C/T snv 0.54 0.010 1.000 1 2019 2019
Congenital small ears
CUI: C0152423
Disease: Congenital small ears
13 0.882 0.160 10 121594355 intron variant C/T snv 0.54 0.010 1 2019 2019