Skip to main content

Table 1 SNPs that show significant differences between the Prakriti groups after FDR correction for multiple testing set at a threshold of significance of p < 0.05

From: Combined genetic effects of EGLN1 and VWF modulate thrombotic outcome in hypoxia revealed by Ayurgenomics approach

Gene

SNP

Variation

Comparison

Allele

Allele frequency 1

Allele frequency 2

P value

Allele frequency (1 vs. 2)

EPR

rs1171271

C/T

PvsK

C

0.46

0.13

5.40E−05

OR6K3

rs857703

A/G

KvsV

A

0.11

0.43

4.44E−05

UCP2

rs660339

A/G

KvsV

A

0.15

0.49

4.23E−05

OLR1

rs3741860

A/G

VvsP

G

0.49

0.14

2.87E−05

OLR1

rs3741860

A/G

PvsK

G

0.14

0.53

6.35E−06

SPTA1

rs857691

C/T

PvsK

T

0.40

0.06

1.63E−05

SPTA1

rs857721

A/T

PvsK

A

0.43

0.05

6.05E−07

VWF

rs1063856

C/T

PvsK

C

0.05

0.37

1.55E−05

OR10Z1

rs857685

A/C

PvsK

C

0.41

0.05

1.46E−06