Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.16 (G)
Location

Chromosome 1:113812320 (forward strand) | View in location tab

Co-located

with COSMIC COSM1560090 (T/G) ; HGMD-PUBLIC CR053507

Most severe consequence
Evidence status

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

1:g.113812320T>G
ENST00000261441.7:c.93A>C
ENST00000612242.2:c.93A>C

This variation has assays on 5 chips - click the plus to show

Variation displays