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Human (GRCh37.p13)
Most severe consequence
 
intergenic variant
Alleles
C/T|Ancestral: C|MAF: 0.08 (T)|Highest population MAF: 0.17
Change tolerance
CADD: T:0.282
Location

Chromosome 2:127866047 (forward strand)|VCF:2  127866047  rs35860453  C  T

Co-located variant

dbSNP rs1573855013 (C/-)

Evidence status

HGVS name

NC_000002.11:g.127866047C>T

Synonyms

ClinGen Allele Registry CA16111299 (T)

Original source

Variants (including SNPs and indels) imported from dbSNP (release 154)|View in dbSNP

About this variant

This variant has 2504 sample genotypes.

Variant displays