Source: ALL

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: rs201140091
rs201140091
FRMPD2
1.000 0.040 10 48200198 intron variant A/-;AAAAA;AAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA delins
CUI: C0027092
Disease: Myopia
Myopia 		0.700 1.000 1 2016 2016
dbSNP: rs745708
rs745708
FRMPD2
1.000 0.080 10 48237632 intron variant A/G snv 0.27
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs115907611
rs115907611
FRMPD2
1.000 0.080 10 48187279 missense variant G/A snv 2.0E-05 2.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 0