Variant report

Variant	rs10487206
Chromosome Location	chr7:104045449-104045450
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1014557	0.83[CHB][hapmap];0.93[JPT][hapmap]
rs10487205	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16869746	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs17137313	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs17137377	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs17137382	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs2188484	0.81[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4605995	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6952192	0.86[ASN][1000 genomes]
rs967919	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs967920	0.93[CHB][hapmap];1.00[JPT][hapmap]

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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