Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 1:229282184 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs342863, rs368446, rs1194065

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2506 individual genotypes.

Variation displays