Most severe consequence
28
intron variant
Alleles
G/C|Ancestral: G|MAF: 0.38 (C)|Highest population MAF: 0.50
Change tolerance
CADD: C:7.269|GERP: 1.15
Location
Chromosome 8:101973785 (forward strand)|VCF:8 101973785 rs1543771 G C
Evidence status 
HGVS names
This variant has 3 HGVS names - Show
Synonyms
ClinGen Allele Registry CA12734473 (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 2 transcripts and has 3009 sample genotypes.
