Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 6:162622197 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM992652

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

Variation displays