Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:42831571 (forward strand) | View in location tab

Co-located

with dbSNP rs67375268 (CTTT/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs67375269

This variation has 5 HGVS names - click the plus to show

Variation displays