Most severe consequence
28
intron variant
Alleles
A/C|Ancestral: A|MAF: 0.36 (A)|Highest population MAF: 0.49
Change tolerance
CADD: C:3.298|GERP: -2.21
Location
Chromosome 12:51685722 (forward strand)|VCF:12 51685722 rs1601012 A C
Evidence status 
HGVS names
This variant has 7 HGVS names - Show
Synonyms
ClinGen Allele Registry CA13687633 (C)
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 6 transcripts, has 2504 sample genotypes and is mentioned in 4 citations.
Description from SNPedia
Description not available [More information from SNPedia]
