Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (T)
Location

Chromosome 1:206944645 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3748675

This variation has 2 HGVS names - click the plus to show

1:g.206944645T>C
ENST00000423557.1:c.225+56A>G

This variation has assays on 4 chips - click the plus to show

Variation displays