Variant report

Variant	rs1325572
Chromosome Location	chrX:55828681-55828682
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1473760	1.00[YRI][hapmap]
rs1473761	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs2375465	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs4826411	1.00[CEU][hapmap]
rs5913857	0.83[LWK][hapmap];1.00[YRI][hapmap]
rs5913859	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs5913861	1.00[CEU][hapmap]
rs5914428	0.83[LWK][hapmap];1.00[YRI][hapmap]
rs5914434	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs5914436	1.00[YRI][hapmap]
rs5914440	1.00[YRI][hapmap]
rs5960093	1.00[YRI][hapmap]
rs5960480	0.84[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs6611425	1.00[CEU][hapmap]
rs6612359	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs7885685	1.00[CEU][hapmap]

No data

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

No data

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

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