chr17:27801555:C>A Detail (hg38)

Information

Genome

Assembly Position
hg19 chr17:26,128,581-26,128,581 View the variant detail on this assembly version.
hg38 chr17:27,801,555-27,801,555

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.060
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 Disorder of Achilles tendon A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) ... BeFree 22588838 Detail
<0.001 Disorder of Achilles tendon A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) ... BeFree 22588838 Detail
<0.001 Tendinopathy A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) ... BeFree 22588838 Detail
<0.001 Tendinopathy A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) ... BeFree 22588838 Detail
<0.001 Tendinopathy A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) ... BeFree 22588838 Detail
Annotation

Annotations

DescrptionSourceLinks
A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) and 199 Australia (A... DisGeNET Detail
A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) and 199 Australia (A... DisGeNET Detail
A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) and 199 Australia (A... DisGeNET Detail
A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) and 199 Australia (A... DisGeNET Detail
A total of 358 unaffected control (CON) participants [159 South Africa (SA CON) and 199 Australia (A... DisGeNET Detail
Gene
-
dbSNP
rs2779249 dbSNP
Genome
hg38
Position
chr17:27,801,555-27,801,555
Variant Type
snv
Reference Allele
C
Alternative Allele
A
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))
rs2779249
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.06
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1005
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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