chr6:88851751:G>A Detail (hg19) (CNR1)

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Information

Genome

Assembly	Position
hg19	chr6:88,851,751-88,851,751
hg38	chr6:88,142,032-88,142,032 View the variant detail on this assembly version.

Summary

Links

Type	Database	ID	Link
Gene	MIM	114610	OMIM
	HGNC	2159	HGNC
	Ensembl	ENSG00000118432	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv26135857	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

[No Data.]

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.004	schizophrenia	In the present study, we investigated three polymorphisms (rs1049353, rs806368, ...	BeFree	21695734	Detail

Annotation

Descrption	Source	Links
In the present study, we investigated three polymorphisms (rs1049353, rs806368, and rs4707436) in th...	DisGeNET	Detail

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs4707436 dbSNP
Genome: hg19
Position: chr6:88,851,751-88,851,751
Variant Type: snv
Reference Allele: G
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)): rs4707436
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831)): 0.0661
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831)): 1107
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831)): 16760

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