Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.06 (A)
Location

Chromosome 1:169467915 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs116971455, rs60335656

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2775 sample genotypes.

Variant displays