Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.23 (G)
Location

Chromosome 6:135105435 (forward strand) | View in location tab

Co-located
Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs61043270

HGVS name

6:g.135105435A>G

This variation has assays on 14 chips - click the plus to show

Variation displays