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Human (GRCh37.p13)
Most severe consequence
 
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]

Variant displays