Source: UNIPROT

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: rs1057519925
rs1057519925
0.683 0.560 3 179210291 missense variant G/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs1057519927
rs1057519927
0.716 0.240 3 179218295 missense variant A/C;G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 0
dbSNP: rs1057519929
rs1057519929
0.776 0.320 3 179199066 missense variant G/A snv
Megalencephaly cutis marmorata telangiectatica congenita
0.700 0
dbSNP: rs1057519930
rs1057519930
1.000 0.080 3 179199142 missense variant G/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs121913273
rs121913273
0.605 0.440 3 179218294 missense variant G/A;C snv
CUI: C2751313
Disease: CLAPO Syndrome
CLAPO Syndrome
0.800 0
dbSNP: rs121913273
rs121913273
0.605 0.440 3 179218294 missense variant G/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs121913273
rs121913273
0.605 0.440 3 179218294 missense variant G/A;C snv
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia
0.700 0
dbSNP: rs121913277
rs121913277
0.925 0.280 3 179234302 missense variant G/A;C snv
Megalencephaly cutis marmorata telangiectatica congenita
0.700 0
dbSNP: rs121913281
rs121913281
0.623 0.520 3 179234296 missense variant C/T snv
Megalencephaly cutis marmorata telangiectatica congenita
0.800 0
dbSNP: rs121913283
rs121913283
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06
Megalencephaly cutis marmorata telangiectatica congenita
0.700 0
dbSNP: rs121913283
rs121913283
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 0
dbSNP: rs121913286
rs121913286
0.677 0.280 3 179218306 missense variant C/A;G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 0
dbSNP: rs121913286
rs121913286
0.677 0.280 3 179218306 missense variant C/A;G snv
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.700 0
dbSNP: rs121913287
rs121913287
0.752 0.400 3 179199088 missense variant G/A snv
Megalencephaly cutis marmorata telangiectatica congenita
0.700 0
dbSNP: rs121913288
rs121913288
1.000 0.200 3 179234219 missense variant A/G snv
Megalencephaly cutis marmorata telangiectatica congenita
0.700 0
dbSNP: rs1242945375
rs1242945375
1.000 0.200 3 179234261 missense variant C/T snv
Megalencephaly cutis marmorata telangiectatica congenita
0.700 0
dbSNP: rs867262025
rs867262025
0.790 0.360 3 179221146 missense variant G/A snv
Megalencephaly cutis marmorata telangiectatica congenita
0.700 0
dbSNP: rs104886003
rs104886003
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 2 2005 2005
dbSNP: rs121913272
rs121913272
0.752 0.400 3 179210192 missense variant T/C;G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 2 2005 2005
dbSNP: rs772110575
rs772110575
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 2 2005 2005
dbSNP: rs397517201
rs397517201
0.732 0.240 3 179218307 missense variant A/C;G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2006 2006
dbSNP: rs104886003
rs104886003
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis
0.800 1.000 1 2007 2007
dbSNP: rs121913274
rs121913274
0.645 0.320 3 179218304 missense variant A/C;G;T snv
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis
0.700 1.000 1 2007 2007
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis
0.800 1.000 1 2007 2007
dbSNP: rs121913273
rs121913273
0.605 0.440 3 179218294 missense variant G/A;C snv
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis
0.710 1.000 0 2007 2007