Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.07 (T)
Location

Chromosome 1:150646372 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1707160

This variation has 4 HGVS names - click the plus to show

Variation displays