Original source

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

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

Chromosome 1:97098598 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM973073

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

1:g.97098598C>T
ENST00000422980.1:n.64+2612C>T
ENST00000370192.4:c.2657G>A
ENSP00000359211.3:p.Arg886His
LRG_722:g.827462G>A
LRG_722t1.1:c.2657G>A
LRG_722p1.1:p.Arg886His

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad, Illumina_1M-duo

Variation displays