Variant report

Variant	rs6990255
Chromosome Location	chr8:34126948-34126949
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1495231	0.85[AFR][1000 genomes]
rs1495234	0.85[AFR][1000 genomes]
rs2590461	0.82[ASN][1000 genomes]
rs2590462	0.82[ASN][1000 genomes]
rs2590465	0.82[ASN][1000 genomes]
rs2590466	0.82[ASN][1000 genomes]
rs2609600	0.82[ASN][1000 genomes]
rs2719299	0.82[ASN][1000 genomes]
rs2719300	0.82[ASN][1000 genomes]
rs2953928	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2978846	0.85[AFR][1000 genomes]

Variant related diseases (count:2)

Disease	PMID	Source
Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)	23453885	GWAS catalog
Bipolar disorder	19416921	GWAS catalog

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34125400-34128400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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