chr1:241792153:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr1:241,792,153-241,803,671
hg38 chr1:241,628,851-241,640,369 

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 choroideremia NA BeFree Detail
0.002 multiple sclerosis NA GAD Detail
<0.001 retinal degeneration NA BeFree Detail
<0.001 allergic asthma NA BeFree Detail
<0.001 Coinfection NA BeFree Detail
<0.001 Usher syndrome type 2 NA BeFree Detail
<0.001 Usher Syndrome, Type II NA BeFree Detail
0.005 asthma NA BeFree,GAD,LHGDN Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA 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
chr1:241,792,153-241,803,671
Variant Type
snv
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