Most severe consequence
7
Start lost
Alleles
A/G|Ancestral: A|MAF: < 0.01 (G)|Highest population MAF: < 0.01
Location
Chromosome 7:130416957 (forward strand)|View in location tab
Co-located variant
HGMD-PUBLIC CM120753
Evidence status 
Clinical significance
HGVS names
This variant has 26 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 16 transcripts, has 2504 sample genotypes and is associated with 3 phenotypes.
Description from SNPedia
Description not available [More information from SNPedia]
