Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.19 (A)
Location

Chromosome 3:171014511 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941277

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 13 chips - click the plus to show

Variation displays