Most severe consequence
21
intron variant
Alleles
G/A/C|Ancestral: A|MAF: 0.22 (C)|Highest population MAF: 0.36
Change tolerance
CADD: A:3.682, C:2.706
Location
Chromosome 2:127852021 (forward strand)|VCF:2 127852021 rs10207628 G A,C
Evidence status 
HGVS names
This variant has 24 HGVS names - Show
Synonyms
This variant has 3 synonyms - Show
Genotyping chips
This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K
Original source
Variants (including SNPs and indels) imported from dbSNP (release 154)|View in dbSNP
About this variant
This variant overlaps 11 transcripts, 1 regulatory feature, has 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]
