Source: BEFREE

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: rs1007541
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs1007541
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2017 2017
dbSNP: rs1007541
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs1007541
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2017 2017