rs113871094, FBN1

N. diseases: 34
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.
Hyperextensible thumb
CUI: C4025148
Disease: Hyperextensible thumb
2 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Round ear
CUI: C4021959
Disease: Round ear
4 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Slender finger
CUI: C1857482
Disease: Slender finger
5 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Heart murmur
CUI: C0018808
Disease: Heart murmur
10 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Smooth philtrum
CUI: C1142533
Disease: Smooth philtrum
10 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Malar flattening
CUI: C1858085
Disease: Malar flattening
12 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Exanthema
CUI: C0015230
Disease: Exanthema
14 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Joint laxity
CUI: C0086437
Disease: Joint laxity
15 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Long philtrum
CUI: C1865014
Disease: Long philtrum
16 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Umbilical hernia
CUI: C0019322
Disease: Umbilical hernia
17 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Relative macrocephaly
CUI: C1849075
Disease: Relative macrocephaly
19 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Weill-Marchesani Syndrome, Autosomal Dominant
CUI: C1869115
Disease: Weill-Marchesani Syndrome, Autosomal Dominant
23 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT
CUI: C3541518
Disease: ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT
24 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Thin upper lip vermilion
CUI: C1865017
Disease: Thin upper lip vermilion
25 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Congenital pectus carinatum
CUI: C0158731
Disease: Congenital pectus carinatum
26 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Stiff Skin Syndrome
CUI: C1861456
Disease: Stiff Skin Syndrome
26 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
GELEOPHYSIC DYSPLASIA 2
CUI: C3280054
Disease: GELEOPHYSIC DYSPLASIA 2
27 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
MARFAN LIPODYSTROPHY SYNDROME
CUI: C4310796
Disease: MARFAN LIPODYSTROPHY SYNDROME
27 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Nasal bridge wide
CUI: C1849367
Disease: Nasal bridge wide
29 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Acromicric Dysplasia
CUI: C0265287
Disease: Acromicric Dysplasia
31 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Congenital diaphragmatic hernia
CUI: C0235833
Disease: Congenital diaphragmatic hernia
31 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
OVERLAP CONNECTIVE TISSUE DISEASE
CUI: C1858556
Disease: OVERLAP CONNECTIVE TISSUE DISEASE
31 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Small hand
CUI: C0575802
Disease: Small hand
31 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Flexion contracture
CUI: C0333068
Disease: Flexion contracture
32 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0
Growth delay
CUI: C0456070
Disease: Growth delay
40 0.683 0.320 15 48465820 stop gained G/A snv 0.700 0