Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.21 (C)
Location

Chromosome 6:135097880 (forward strand) | View in location tab

Co-located
Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61446782

This variation has 2 HGVS names - click the plus to show

6:g.135097880T>C
ENST00000529882.2:c.88+5048A>G

This variation has assays on 10 chips - click the plus to show

Variation displays