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: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
29 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs174535
rs174535
MYRF ; TMEM258
19 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 0.700 1.000 1 2015 2015
dbSNP: rs174549
rs174549
FADS1 ; FADS2
12 0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.700 1.000 1 2013 2013
dbSNP: rs174550
rs174550
FADS1 ; FADS2
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs174556
rs174556
FADS1 ; FADS2
7 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs13431652
rs13431652
SPC25
5 0.925 0.080 2 168896905 intron variant T/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs174541
rs174541
FADS2
8 1.000 0.080 11 61798436 intron variant T/C snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs174545
rs174545
FADS1 ; FADS2
5 1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs174601
rs174601
FADS2
12 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs334809
rs334809
IL5RA
4 0.925 0.080 3 3088537 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs603424
rs603424
PKD2L1
13 1.000 0.080 10 100315722 intron variant G/A snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs2880301
rs2880301
TPTE2
4 1.000 0.040 13 19526394 intron variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs10237735
rs10237735
PDE1C
2 7 32337136 intron variant C/T snv 7.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs10414689
rs10414689 		2 19 51293045 regulatory region variant T/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs10502435
rs10502435
GREB1L
1 18 21527130 downstream gene variant C/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs10518201
rs10518201
LOC101928893
1 4 78730706 regulatory region variant A/G snv 6.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs10518202
rs10518202 		1 4 78758523 intergenic variant G/T snv 9.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs10809457
rs10809457
LOC105375974
2 9 11402319 intron variant G/T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs11038747
rs11038747
PHF21A
1 11 46036689 intron variant T/C snv 1.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs11038755
rs11038755
PHF21A
1 11 46057150 intron variant A/G snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs11038756
rs11038756
PHF21A
1 11 46057507 intron variant T/C snv 2.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs11038764
rs11038764
PHF21A
1 11 46098201 intron variant G/A snv 3.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs11083274
rs11083274
ABHD3
1 18 21677162 intron variant T/C snv 0.15 0.700 1.000 1 2018 2018