chr10:18129993:G>A Detail (hg19)

Information

Genome

Assembly Position
hg19 chr10:18,129,993-18,129,993
hg38 chr10:17,841,064-17,841,064 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

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 Leprosy, Multibacillary However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... BeFree 22392581 Detail
<0.001 Leprosy, Multibacillary However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... BeFree 22392581 Detail
<0.001 Leprosy, Paucibacillary However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... BeFree 22392581 Detail
Annotation

Annotations

DescrptionSourceLinks
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... DisGeNET Detail
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... DisGeNET Detail
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... DisGeNET Detail
Gene
-
dbSNP
rs692527 dbSNP
Genome
hg19
Position
chr10:18,129,993-18,129,993
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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