RAB5C, RAB5C, member RAS oncogene family, 5878

N. diseases: 24; N. variants: 18
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7224737
rs7224737
17 42137346 intron variant G/A snv 0.36
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 2 2016 2017
dbSNP: rs11079034
rs11079034
17 42136872 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs11079035
rs11079035
1.000 0.040 17 42136994 intron variant G/A snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs11079035
rs11079035
1.000 0.040 17 42136994 intron variant G/A snv 0.29
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs11079035
rs11079035
1.000 0.040 17 42136994 intron variant G/A snv 0.29
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12325861
rs12325861
1.000 0.040 17 42137394 intron variant T/A;C snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12603327
rs12603327
17 42138534 intron variant T/C snv 0.37
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs12603330
rs12603330
17 42138571 intron variant T/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs13380830
rs13380830
0.882 17 42145640 intron variant C/G snv 0.29
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2019 2019
dbSNP: rs13380830
rs13380830
0.882 17 42145640 intron variant C/G snv 0.29
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs13380830
rs13380830
0.882 17 42145640 intron variant C/G snv 0.29
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2019 2019
dbSNP: rs13380830
rs13380830
0.882 17 42145640 intron variant C/G snv 0.29
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2019 2019
dbSNP: rs1869365
rs1869365
17 42141847 intron variant T/C snv 0.40
CUI: C2825857
Disease: Factor VIII measurement
Factor VIII measurement
0.700 1.000 1 2019 2019
dbSNP: rs1869365
rs1869365
17 42141847 intron variant T/C snv 0.40
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2019 2019
dbSNP: rs2240009
rs2240009
17 42131124 intron variant C/G snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7214921
rs7214921
17 42142007 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs7224737
rs7224737
17 42137346 intron variant G/A snv 0.36
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2012 2012
dbSNP: rs7224737
rs7224737
17 42137346 intron variant G/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs739636
rs739636
17 42129045 intron variant T/G snv 0.40
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs739637
rs739637
17 42128926 intron variant G/C snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs78862468
rs78862468
17 42135088 intron variant C/T snv 3.8E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs8070446
rs8070446
17 42133861 intron variant G/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs8074708
rs8074708
17 42134336 intron variant G/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9903204
rs9903204
17 42136044 intron variant G/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9915255
rs9915255
17 42132173 intron variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013