Most severe consequence
21
Intron variant
Alleles
T/C|Ancestral: C|MAF: 0.44 (T)|Highest population MAF: 0.50
Location
Chromosome 7:11563272 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
Archive dbSNP rs61686367
Genotyping chips
This variant has assays on 9 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 2 transcripts, has 3748 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.