Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 1:155289124 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs185632402

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays