Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 6:18122402 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033789

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

6:g.18122402G>C
ENST00000340650.4:c.205C>G
ENSP00000345464.3:p.Pro69Ala

Variation displays