Variant report

Variant	rs12433909
Chromosome Location	chr14:63378192-63378193
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10459522	1.00[YRI][hapmap]
rs11846438	0.92[CEU][hapmap]
rs12431729	0.83[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap]
rs12882531	1.00[YRI][hapmap]
rs12883703	0.92[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap]
rs1956016	0.81[CHB][hapmap]
rs1980561	0.92[CEU][hapmap];0.80[JPT][hapmap]
rs34487983	0.84[EUR][1000 genomes]
rs71414475	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

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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