Most severe consequence
21
Intron variant
Alleles
C/T|Ancestral: C
Location
Chromosome 7:92209796 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 15 HGVS names - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 9 transcripts and is mentioned in 1 citation.
