Variant report

Variant	rs797168
Chromosome Location	chr12:10882349-10882350
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10772356	0.92[CEU][hapmap];0.82[CHB][hapmap];0.86[CHD][hapmap];0.91[MEX][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes]
rs10845210	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1126501	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6488323	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs797169	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10878600-10884000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

Quick Search:

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

what's new

Quick links