rs761051758, HSPB1

N. diseases: 7
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.
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 0.030 1.000 3 2004 2019
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 0.010 1.000 1 2007 2007
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 0.010 1.000 1 2007 2007
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
87 0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 0.010 1.000 1 2004 2004
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 0.010 1.000 1 2007 2007
Paresis
CUI: C0030552
Disease: Paresis
49 0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 0.010 1.000 1 2004 2004
Spinal Cord Ischemia
CUI: C0752130
Disease: Spinal Cord Ischemia
3 0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 0.010 1 2008 2008