Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.15 (A)
Location

Chromosome 6:137320996 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59766138, rs1744050

HGVS name

6:g.137320996A>T

Variation displays