Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.34 (C)
Location

Chromosome 11:60852184 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR042843

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs1224037, rs57414459

HGVS names

This variant has 2 HGVS names - Hide

11:g.60852184T>C
ENST00000332539.4:c.*351A>G

About this variant

This variant overlaps 5 transcripts, has 2510 sample genotypes and is mentioned in 4 citations.

Variant displays