chr20:6786464:A>G Detail (hg38) (BMP2)

Information

Genome

Assembly Position
hg19 chr20:6,767,111-6,767,111 View the variant detail on this assembly version.
hg38 chr20:6,786,464-6,786,464

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.102
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance confers sensitivity
Review star
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
confers sensitivity 2012-05-01 criteria provided, single submitter lung cancer germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.003 iron deficiency anemia To evaluate the association of genetic variants in genes involved in iron delive... BeFree 22323359 Detail
0.003 Hereditary hemochromatosis Our results make it likely the role of rs10421768, rs235756, rs2230267 and rs143... BeFree 25976471 Detail
<0.001 Hereditary hemochromatosis We investigated 6 polymorphisms (rs10421768 in HAMP gene, rs235756 in BMP2 gene,... BeFree 25976471 Detail
0.125 Hereditary hemochromatosis We investigated 6 polymorphisms (rs10421768 in HAMP gene, rs235756 in BMP2 gene,... BeFree 25976471 Detail
Annotation

Annotations

DescrptionSourceLinks
NC_000020.11:g.6786464A>G AND Lung cancer ClinVar Detail
To evaluate the association of genetic variants in genes involved in iron delivery and hepcidin regu... DisGeNET Detail
Our results make it likely the role of rs10421768, rs235756, rs2230267 and rs1439816 polymorphisms, ... DisGeNET Detail
We investigated 6 polymorphisms (rs10421768 in HAMP gene, rs235756 in BMP2 gene, rs2230267 in FTL ge... DisGeNET Detail
We investigated 6 polymorphisms (rs10421768 in HAMP gene, rs235756 in BMP2 gene, rs2230267 in FTL ge... DisGeNET Detail
Gene
-
dbSNP
rs235756 dbSNP
Genome
hg38
Position
chr20:6,786,464-6,786,464
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))
rs235756
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.1023
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1715
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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