Most severe consequence
21
Intron variant
Alleles
C/T|Ancestral: C|MAF: 0.06 (T)|Highest population MAF: 0.27
Location
Chromosome 7:92779015 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 8 HGVS names - Show
Synonyms
Archive dbSNP rs17696703, rs57523974
Genotyping chips
This variant has assays on 8 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 4 transcripts, 1 regulatory feature, has 3904 sample genotypes and is mentioned in 5 citations.
Description from SNPedia
Description not available [More information from SNPedia]
