Most severe consequence
5
frameshift variant
Alleles
TTT/TT|Ancestral: TTT|Highest population MAF: < 0.01
Location
Chromosome 13:36903553-36903555 (forward strand)|VCF:13 36903553 rs1060499524 TT T
Evidence status 
Clinical significance
HGVS names
This variant has 10 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant overlaps 5 transcripts, is associated with 2 phenotypes and is mentioned in 4 citations.
Description from SNPedia
Description not available [More information from SNPedia]