This variant has been flagged

  • None of the variant alleles match the reference allele (AA)
  • Mapped position is not compatible with reported alleles
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ambiguity code: R
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence (AA) at this location.
Location

Chromosome 11:71441066-71441067 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17161513, rs760239

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 26 transcripts and has 39 sample genotypes.

Variant displays