Most severe consequence
4
Stop gained
Alleles
C/A|Ancestral: C
Location
Chromosome 16:55485677 (forward strand)|View in location tab
Co-located variant
HGMD-PUBLIC CM012156
Evidence status 
Clinical significance
HGVS names
This variant has 21 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 8 transcripts and is associated with 2 phenotypes.
Description from SNPedia
Description not available [More information from SNPedia]
