chr5:160467840:A>G Detail (hg38)

Information

Genome

Assembly Position
hg19 chr5:159,894,847-159,894,847 View the variant detail on this assembly version.
hg38 chr5:160,467,840-160,467,840

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.169
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[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 Sepsis Our study has analyzed the association of sepsis with two functional miR-146a ge... BeFree 24701036 Detail
<0.001 Septicemia Our study has analyzed the association of sepsis with two functional miR-146a ge... BeFree 24701036 Detail
Annotation

Annotations

DescrptionSourceLinks
Our study has analyzed the association of sepsis with two functional miR-146a gene SNPs rs2910164 G/... DisGeNET Detail
Our study has analyzed the association of sepsis with two functional miR-146a gene SNPs rs2910164 G/... DisGeNET Detail
Gene
-
dbSNP
rs57095329 dbSNP
Genome
hg38
Position
chr5:160,467,840-160,467,840
Variant Type
snv
Reference Allele
A
Alternative Allele
G
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs57095329
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.1694
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
2839
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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