Original source

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

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

Chromosome 1:236885202 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961002

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

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

Variation displays