chr4:166248821:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr4:166,248,821-166,264,316
hg38 chr4:165,327,669-165,343,164 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Diabetes Mellitus, Non-Insulin-Dependent NA BeFree Detail
<0.001 cataract Significantly, 8/36 (22%) DRGs are associated with cataracts in human (GSTO1, MG... BeFree 25896808 Detail
<0.001 Dyslipidemias NA BeFree Detail
<0.001 Psoriasiform eczema NA BeFree Detail
<0.001 Developmental delay (disorder) NA BeFree Detail
<0.001 Bilateral cataracts (disorder) Significantly, 8/36 (22%) DRGs are associated with cataracts in human (GSTO1, MG... BeFree 25896808 Detail
<0.001 CK syndrome NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
Significantly, 8/36 (22%) DRGs are associated with cataracts in human (GSTO1, MGST1, SC4MOL, UCHL1) ... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Significantly, 8/36 (22%) DRGs are associated with cataracts in human (GSTO1, MGST1, SC4MOL, UCHL1) ... DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chr4:166,248,821-166,264,316
Variant Type
snv
Genome browser